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Biomedical Waste Collection, Transportation, Treatment, Storage and Disposal Facility Mumbai, Maharashtra,

INDIA

MANAGEMENT OF BIOMEDICAL WASTE:

COLLECTION, TRANSPORTATION, TREATMENT,

STORAGE & DISPOSAL FACILITY,AT MUMBAI

REQUEST FOR PROPOSAL (RFP) DOCUMENT

PART 2 PROJECT SCOPE

NOVEMBER 2004

MAHARASHTRA POLLUTION CONROL BOARD

MUMBAI

Request for Proposal Part 2 Project Scope 1


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TABLE OF CONTENTS

1. DEFINITIONS ............................................................................................................................................ 32. PROJECT SCOPE......................................................................................................................................43. REQUEST FOR PROPOSALS................................................................................................................. 64. ONGOING BIOMEDICAL WASTE MANAGEMENT PROJECTS IN MPCB

INDUSTRIAL AREAS............................................................................................................................... 75. ESTIMATEDQUANTITES OF BIOMEDICAL WASTE GENERATED IN MCGM AREAS AS

PER BMWM RULES................................................................................................................................ 86. ELEMENTS OF THE BMWTSDF AND THEIR PHYSICAL SPECIFICATIONS .........................136.1 MONITORING.126.2 PRELIMINARY TREATMENT FACILITIES................................................................................................146.3 COMPOSITE BIOMEDICAL WASTES INCINERATOR/PGV REACTOR/CLOS REACTOR........................14

7. TREATMENT STANDARDS/WASTE ACCEPTANCE CRITERIA FOR BMWTSDF..................19

7.1 INTRODUCTION ......................................................................................................................................197.2 NOISE .....................................................................................................................................................257.3 AESTHETICS...........................................................................................................................................257.4 NOTIFICATION OF COMPLLIANCE25

8. CRITERIA FOR SEGREGATION, COLLECTION AND TRANSPORTATION OF BMW26



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1. DEFINITIONS1 Charges: Tariffs charged by Operator of the BMWTSDF for daily collection,

transportation, handling, storage, preliminary & final treatment, of wastes intoIncinerator/steam Sterilization /Microwave, shredder at BMWTSDF as well as

transportation and disposal of Incinerator ash/residue/reject solids from shreederinto Secured Landfill Facility (TSDF) developed as per the Hazardous Waste (M&H)Rules 1989. The tariffs would be as per category of waste and would cover the costsof setting up, operation and maintenance of BMWTSDF, and acceptable profits.

2 BMWTSDF: Biomedical Waste Collection, Transport, Treatment, Storage andDisposal Facility

3 CPCB: Central Pollution Control Board4 EIA: Environmental Impact Assessment5 EC: European Commission6 Establishment: Planning, designing, financing, procurement of raw materials, and

construction of the BMWTSDF as specified in this Request For Proposal documentand as per CPCB/MoEF/MPCB guidelines and authorisations.

7 Facility: The premises / HCE/ where Biomedical wastes are produced.8 Generator: The HCE generating / producing Bio-medical wastes.9 Biomedical wastes: As specified in Biomedical Waste (Management and Handling)

Rules, 1998 as amended.

10 HW Rules: Hazardous Wastes (Management & Handling) Rules, 1989, framedunder the Environment (Protection) Act, 1986, as amended.

11 MPCB: Maharashtra Pollution Control Board12 MCGM: Municipal Corporation of Greater Mumbai13 MoEF: Ministry of Environment & Forests14 Developer/Operator: The agency collecting, storing, treating and disposing the

Biomedical waste at the proposed BMWTSDF.

15 USEPA: United States Environmental Protection Agency16 BOOT: Build, Own, Operate and Transfer.



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2. PROJECT SCOPEA)The Operator is expected to be responsible for the following as part of establishing

and operating the Project:

1 Establishment of the BMWTSDF as per specifications laid down in Section 62 Daily Transportation of Biomedical waste from Generators facility to the

BMWTSDF.

3 Inspection of Biomedical waste as per the manifest system prescribed under theauthorisation issued by MPCB to the Generator in respect of class of waste, quantumof waste, method of treatment and disposal there under at the Generators facilityand acceptance for preliminary investigations at the BMWTSDF.

4 Carrying out Collection, Transport, Treatment, Storage and Disposal of Biomedicalwaste.

5 Collection of Charges from Generator There has to be some sort of centralcollection point.

6 Transportation of residue/rejects/ash generated from Incineration and solids fromshreeder to TSDF developed as per Hazardous Waste Rules for disposal.

7 Monitoring on-site and off-site including emergency preparedness. (Monitoring,safety & security, contingency plan, risk management and emergency procedures).

8 Reporting to regulatory authorities needed. (Record keeping).9 Carrying out Public information and consultation, prior to construction, during

construction, and operations. (Public Consultation).

10 Monitoring of the emissions from the Incinerator Air Pollution Control System(APCS)/performance of the gas clearing system.11 Transfer of BMWTSDF after 20 years to MCGM (Lesser of the land on which the

BMWTSDF is to be Established), after satisfactory compliance of the BMWTSDF asper the MPCB authorisation.

12 Establishment and operations of the BMWTSDF have to comply with inter alia,MoEF/ CPCB/MPCB guidelines, Biomedical Waste (Management and Handling)Rules, 1998, as amended 2003.

13 All civil structures in facility should be constructed as per relevant IS code/s inconsultation with technology providers. The structural designs of all buildingsshould be got approved from IIT Mumbai or Consultant appointed by MCGM.Bidder should also quote block rates of shed / buildings etc per Sq.mt.

14 MCGM Chief Engineer will supervise the work. The work should be executed as perhis instructions. Before executing the work all drawings /designs for FSI calculationshould be got approved from competent authority of MCGM & all workingdrawings should be submitted to component authority. MCGM shall carry out



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Quality Audit of works to keep close control & vigilance on works from qualitypoint of view.

15 The operator of the facility shall be operating the facility for 20 Years period fromthe date of commissioning of this facility and shall transfer the same to MCGM ingood working condition after the expire of 20 years period. After the BOOT Periodof 20 years period MCGM may decide the new operator of the facility or maycontinue with the existing operator of the facility depending uponcondition/situation at that time.



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Bio

IN

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medical Waste Collection, Transportation, Treatment, Storage and Disposal Facility Mumbai, Maharashtra,

DIA

equest for Proposal Part 2 Project Scope 6

3. REQUEST FOR PROPOSALSA)Municipal Corporation of Greater Mumbai is an urban local body, responsible for

facilitating development of common facilities for collection, transport, treatment,storage and disposal of bio-medical wastes as per Biomedical wastes (Management

& Handling) Rules,1998, as amended.

B) In compliance of he Bio-Medical Waste (Management & Handling) Rules 1998, asamended, MCGM has proposed to develop Integrated Biomedical Waste, Collection,transport, Treatment & Disposal Facility at E W and Mumbai city (Central)Zones of Mumbai on Plots admeasuring --------,-------,--------acres in the Corporationlimit of MUMBAI, Maharashtra, for management of Biomedical Waste generatedfrom HCEs such as hospitals, nursing homes, clinics, dispensaries, Veterinaryinstitutions, animal houses, pathological laboratories, blood banks etc. located inMCGM area Mumbai. A table showing estimated quantities of Biomedical wastegenerated zone wise is enclosed.

C) Integrated BMWTSDF site shall be as per:1 The minimum physical specifications as given in Section 6.2 The minimum treatment standards/waste acceptance criteria to be followed by

the operator for the proposed facility, as specified in Section 7, as well asguidelines/authorisations of CPCB/MoEF/MPCB.

3 The Operating/Performance Requirements of BMWTSDF.D)The guidelines prescribed by CPCB for Biomedical waste requiring segregation

before disposal by Incineration/Steam sterilization/Micro waving will have to meet

general emission standards/ambient air quality standards, as enclosed in Section 7.

E) The Techno-Business Proposal submitted by the successful bidder in line with thePart 2 - Project Scope of the RFP and as asked for in the Part 1 - Request forProposal documents, shall be included as a part of the Agreement to be signed bythe Operator and made binding.


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medical Waste Collection, Transportation, Treatment, Storage and Disposal Facility Mumbai, Maharashtra, INDIA

equest for Proposal Part 2 Project Scope

Sr.No. Site Area S t a t u s Facility

1 G.T. HOSPITAL MUMBAI IN OPERATION Incineration

2 TATA HOSPITAL MUMBAI IN OPERATION Hydroclave

3 LILAVATI MUMBAI IN OPERATION Incineration

4 J.J. HOSPITAL MUMBAI IN OPERATION Incineration

5 CAMA MUMBAI IN OPERATION Incineration

6 G.T.B. HOSPITAL MUMBAI IN OPERATION Incineration

4. ONGOING BIOMEDICAL WASTE MANAGEMENT PROJECTSIN MCGM AND NEAR BY AREAS


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5. ESTIMATED QUANTITES OF BIOMEDICAL WASTE GENERATED IN MCGMAREAS AS PER BMWM RULES

Waste Quantity in MT/YrSr.No Zone App.Number

of beds

App. Numberof beds @ 80%occupancy

Total waste Incinerable Other W

1 East 10,000 8000 875

(700)

350

(280)

525

(420)

2 West 10,000 8000 875

(700)

350

(280)

525

(420)

3 Central 10,000 8000 875

(700)

350

(280)

525

(420)

NOTE-

* Figures in parenthesis shows biomedical waste generation with 80% Occupancy

** Estimation based on 250 gm/bed/day of bio-medical waste generation.

***The bidder are requested to carryout independent survey of health careestablishments (HCEs) such as hospitals, Nursing homes, Clinics, dispensaries,Veterinary Institutions, slaughter/animal houses, pathological laboratory/Blood

Bank, Eye-Bank, Semen Bank, Dental clinic, transplant center etc. to get idea ofquantum of bio-medical waste generated.



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5.1 SCHEDULE OF RATES FOR VARIOUS CATEGORIES OF

BIO-MEDICAL WASTE

Sr.

No

Category Basic

Rate inRs.

Unit Remarks

1. Generation of bio-medicalwaste from Hospitals &Nursing homes with beds

I) 1 to 50

II) 51 and above5/-

4/-

Per bed/ day

Per bed/ day

2. Generation of bio-medicalwaste (@ 1 Kg/day)without bed fromfollowing.

Clinic, Dispensaries, DentalClinic, PathologyLaboratories, Bio-ResearchLaboratories, Blood Bank,Eye-Bank, Semen Bank,Transplant Center etc.

350

500

1000

2000

Lumsump/month

Lumsump/month

Lumsump/month

Lumsump/month

C.I**. < 50 Lakhs

C.I. 50 Lakh -1Cr

C.I. 1 Cr* 2 Cr*

C.I**. > 2 Cr*

3. Generation of bio-medicalwaste from following.

Veterinary Institutions/hospital/ College/Education & ResearchInstitute/ all laboratorieswhere animals are rearedor/killed or used foreducation or researchpurpose.

18/- Per Kg/ day

* Cr - Rs. In Crores ** C.I. Capital Investment

I/We hereby submit RFP for above stated rates for Maharashtra Pollution ControlBoard (hereinafter referred to as MPCB) at

(in figures)___________________________________percent above/below.

(in words)___________________________________ percent above/below.



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The estimated rates entered in Schedule (Memorandum showing items of work to becarried out as per the RFP) & in accordance with all specifications, designs,drawings, instructions & rules, terms & conditions of contract as hereinabove &hereinafter included in these RFP documents.

Should this RFP be accepted, I/We hereby agree to abide by & fulfill all the terms &conditions of contract & Principles of Agreement Part-3 annexed hereto, & in defaultthereof to forfeit & pay to Maharashtra Pollution Control Board the sums of moneymentioned in the said RFP.

NOTE: -

(i) All above rates should be inclusive of daily collection, transportation, handlingincineration, Steam sterilization, shredding, disposal of incineration ash/residue/rejects, solid residue from shredder into Secured Engineered LandfillFacility (TSDF) developed as per the Hazardous Waste (Management & Handling)Rules 1989 as amended.

If the variation in rate(s) quoted by the bidder is beyond +10%, brief reasons shall begiven by the bidder separately.

(ii) Above basic rates are estimated considering the present market rates.

(iii) The bidder are requested to carryout independent survey of health careestablishments (HCEs) such as hospitals, Nursing homes, Clinics, dispensaries,Veterinary Institutions, slaughter/animal houses, pathological laboratory/BloodBank, Eye-Bank, Semen Bank, Dental clinic, transplant center etc. to get idea ofquantum of bio-medical waste generated.

(iv)It has been decided that tariff shall not exceed Rs.5 per bed/day with 80%occupancy. Bidder shall offer differential type/ categories of HCEs (e.g.Gyanecology, Orthopaedic, Pathology labs etc.) and quantity of waste generated (e.g.higher quantity lower rate and vice versa).

(v) Tariff/Rate shall be valid for 1 year. Price escalation shall be considered byMCGM based on the advise of the Expert Committee.

(vi) Since MCGM is providing land at nominal cost of Re 1/- per sq meter per yearinitially for 20 Years, a discount of 7% on the tariffs shall be provided for BMW fromHCEs of MCGM.

(vii) The bidders are requested to quote tariffs for each year of the term of theagreement for each of the individual charges as per the Format given in Section 24.

(vii) It is advisable for the operator to introduce a system of checks and balancesto..

(a) Ensure that only bio-medical wastes being given for the treatment bythe generators.



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(b) Calculate in parallel what the per Kg treatment cost would be.

(c) Bring the above (a) and (b) to the notice of generators at the time ofprice review.

5.2 MEMORANDUM

a) Name of Work: - Selection of a Developer for Planning, Design, Finance,Construction, Operation, Maintenance and Transfer of Biomedical WasteCollection, Treatment, Storage and Disposal Facility (BMWTSDF) at one of thethree to four E W, Mumbai city (Central) Zone of MCGM, Mumbai,Maharashtra, India on Build, Own, Operate & Transfer (after 20 years) Basis.

b) Estimated Cost It is BOOT Project. Developer isrequested to Quote minimum CapitalCost.

c) Bid-Security Rs.1, 00,000/-



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d) Development Guarantee Rs.15, 00,000/-

e) BOOT Period 20 Years

f) Standards/Specifications ofequipment to be installed forproject

As per Biomedical Waste (Management& Handling) Rules, 1998, as amended,and given in RFP.

g) Time allowed for the completionof work from the date of signingof agreement with successfulbidder.

4 months excluding monsoon.

h) Compensation for non-completionof work in time/slow progress of

work, for every day the work iscarried out at disproportionatelyslow rate

Rs.1000/- per day



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6. ELEMENTS OF THE BMWTSDF AND THEIR PHYSICAL SPECIFICATIONSThis section details the units that should be physically present in the proposedBMWTSDF. They should comprise:

Segregated storages Laboratory, if required. Steam Sterilisation / shredding Incineration Sharp pit/Encapsulation Facility if required, depending on choice of steam-

steriliser and level of physical disfigurement.

Vehicle /Container Washing Facility Air Pollution Control System (APCS)/Gas Clearing System. Disposal methods for residuals/rejects/incineration ash, solids from shredding Transport facilities Supporting infrastructure Waste water treatment plant depending on choice of steam-steriliser (eg;

required for vacuum autoclaves)

The Operator has to ensure that all units/elements of BMWTSDF, as required underMoEF and CPCB guidelines and MPCB regulations, should be established within theproposed BMWTSDF site.

6.1 Monitoring: -Monitoring equipment for water, air and meteorological parameters will have tobe established as may be stipulated by MPCB. Minimum equipment for thiscould be:

1 Water sampling equipment.2 Stack monitoring kit for analysis of emission of Incinerator to measure

hydrocarbons, carbon monoxide, SO2 (Sulphur dioxide) and particulate matter,Oxides of Nitrogen etc.

3 High volume air sampler for monitoring ambient air quality levels for suspendedparticulate matter, and gaseous air pollutants.

4 Decibel meter to measure noise levels5 Soil testing kit with sampling devices.6 Meteorological equipment such as wind monitor, hygrometer, thermometer etc.7 Spore test and spore validation equipment.



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8 Stack Monitoring Kit9 Proper record keeping and an early warning system are essential components

and have to be taken care of.

6.2Preliminary treatment facilities

A) In the layout, the Operator should offset appropriate area for segregation ofincoming waste, keeping separately, wastes suitable for sorting out for furtherrecovery.

B) Preliminary treatment (no chlorine-based) should be considered in the preliminarytreatment plan of the Operator. Dimensioning shall depend on individual biddersdesign and technology. This becomes necessary specially if waste is stored untreatedin hot weather conditions.

C) Odour mitigation measures would be appreciated.6.3 Composite Biomedical Wastes Incinerator6.3.1 PurposeA)The Incinerator is required for Incineration of Biomedical wastes as defined and

listed in Biomedical Waste (Management & Handling) Rules, 1998, as amended.

6.3.2 Minimum Commissioning Capacity of IncineratorA)The Minimum Commissioning Capacity of the Incinerator should be 100 Kg per

hour. The Incinerator should have the necessary stack height and scrubber facilitiesto meet the emission standards. Operators are free to provide Incinerator withcapacities greater than the commissioning capacity i.e., 100 Kg per hour subject tomeeting all norms, specification and regulations under inter alia Biomedical Waste(Management and Handling) Rules, 1998, as amended.

6.3.3 Physical Specifications for the Incinerator6.3.3.1 General characteristicsA)The Incinerator chambers (primary & secondary) shall be compact, rotary

type/furnace, lined with refractory and insulation furnace connected with flue gaschimney of height of at least 30 meters.

B) The Incinerator should be fired with additive/supplementary clean fuel having alow backup time and conforming to the specified emission norms.

C) The Incinerator should be capable of operating at severe operating conditions in theambient temperature range 15-45 Degrees Centigrade and moisture content of 95%or more.



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D)The Incinerator shall be designed to incinerate bio-medical waste with minimumcapacity 100 Kg per hour

E) The Incinerator should be capable of burning the waste to sterileash/residue/rejects. It should emit smoke free flue gases.

6.3.3.2 Technical featuresA)The Incinerator should be rotary kiln type or fixed furnace lined with high-grade

refractory bricks capable of withstanding a minimum temperature of 1500 deg. C.

B) In the rotary kiln fixed furnace, temperature controller should maintain a minimumtemperature of 850 + 50 deg. C. Controlled flow of air should be maintained forcomplete volatization of solid waste.

C) In the secondary chamber the temperature should be maintained at a minimum of1200 +50 deg. C by the temperature controllers. Here complete combustion should

take place and all smoke produced in the primary chamber shall also get burntcompletely. Residence time in secondary chamber should be a minimum of 1 or 2second so as to bring complete combustion of volatile matter evolved from primarycombustion chamber, with minimum 3 % oxygen in the stack gas.

D)The flue gases from the secondary chamber should pass through the air pollutioncontrol system. The system should be designed to remove pollutants and particulatematter present in the flue gases from secondary chamber. Suitably designedpollution control devices should be installed with the incinerator to achieve theemission limits. In any circumstances the chlorinated plastics shall not beincinerated. The emission level of the exhaust gas should meet the emission norms

as given in the Consent given by MPCB. This system should also bring down theoutlet temperature of flue gases to approx. 80 deg. C before releasing in ambient air,by using air blower etc.

E) There may be two firing systems, fully automatic type, of suitable capacityattached/provided one each for kiln and secondary Incinerator chamber. Theseburners shall be of standard make pressure atomised type, capable of maintainingthe temperature uniform inside the chambers.

F) The kiln and secondary chamber of the Incinerator shall be made of mild steelconforming to IS: 2062 and of suitable thickness lined with high grade refractory and

insulation.

G)The unit shall run on excessive air to ensure fast and complete burning of wastes.The blower shall have the capability to provide the appropriate supply ofcombustion air as well as to dilute the flue gases.

H)Exit doors for ash/residue/rejects removal shall be provided at suitable place oneeach on primary and secondary chamber of the Incinerator.



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I) The waste charging shall have provisions for automatic loading.J) Easily operable charging door shall be provided to facilitate easy loading.K) The charging door should be fitted with limit switches, which in turn shall cut off

the burner in the primary chamber and shall provide all safety measures to the

operator while charging.

L) There shall be no waste accumulation inside the Incinerator to ensure smoothworking.

M)The control panel housing should be of reputed make and button, starters andcontactors shall have digital temperature controls. The on off switch shall have lightindication etc.

N)Heavy metals, if incinerated along with the waste shall come back intoash/residue/rejects for disposal. Toxic meals in he incineration ash shall be limited

with in the regulatory quantities as defined under the Hazardous Waste(Management & handling) Rules 1989 and as amended.

O)The supplier should mention the approximate fuel consumption/ton forincinerating Biomedical waste of the prescribed calorific value corresponding to thecommissioning capacity. Only the low sulphur fuel like LDO, LSHS shall be used asfuel in the incinerator.

P) The power/electrical consumption for the same should also be mentionedseparately.

Q)A chimney of minimum 30-meter height with conical base should be provided alongwith Incinerator. The chimney should be provided with sampling platform, ladder,sampling port, lighting arrangement with proper earthing etc. The design of thechimney shall have to be approved from MPCB/under Boiler, Smoke and NuisanceAct. The chimney should be able to withstand temperatures up to 2400 deg. C.

R) The Incinerator shall be provided with suitable lifting lugs for maintenance purpose,as required.

S) The Incinerator shall have a window fitted with 50 mm safety view glass in both thechambers for viewing.

T) The residence time for the flow gases should not be less than 1 seconds to achievecomplete combustion in SCC with minimum 3% oxygen in the stack gas.

U)Sampling platform should be provided as per CPCB norms to collect stack samplesfrom the chimney for monitoring the air pollutants, if and when required. Holes tobe provided on chimney as per standard CPCB norms against diametriccalculations.



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V) The FD fan should be centrifugal type, having standard make suitable power motorof suitable material.

W)The I.D. fan should be centrifugal type, with suitable power motor to meet witheffective control of emission from chimney.

X) The venturi scrubber and wet scrubber unit shall be of high-energy type of stainlesssteel - 316 make. The scrubbing medium should be water with 5% causticapproximately. It should bring the outlet temperature of gas to 80 deg .C.

Y) A cyclonic type droplet separator made out of 8mm thickness MS plate lined with3mm neoprene rubber should be provided to separate water droplet from the fluegases.

Z) Recirculation pumps of appropriate capacity and of standard make motor should beprovided for recirculation of scrubbing medium.

AA)Oil service tank capacity of 1000 litres made out of 5mm thick MS plate completewith piping along with required MS supporting structure, control valve and fuelindicators/gauge, fuel lifting pumps etc. should be provided.

BB) The whole equipment should be painted with two coats of heat resistantAluminium paint.

CC)Any other necessary system required to bring the flue gas parameters within limitsas per Central/State Pollution Control Board norms should be provided.

DD)The developer shall provide all civil works drawing for Incinerator roomfoundation of chimney and static water tank etc. and get it approved from

competent authority of MCGM.

EE) An effluent treatment plant should be provided for the treatment of effluents at thedischarge point so that the discharge waste water comply with the GeneralStandards of Waste Water Quality notified under the Environment (Protection) Act,1986.

6.3.3.3 Technical SpecificationsA)Material to be incinerated: Composite solid /semi-solid/liquid Biomedical wastes as

defined and listed in Biomedical Waste (Management & Handling) Rules, 1998, asamended.

B) Waste burning capacity: Should be capable of burning minimum 100 Kg/hr.C) Operational hours of the Incineration/gasification per day: Generally 24 hours per

day, for about 300 days during the year.

D)Additional filters/separation capacities: The operator shall furnish specific featuresif any regarding additional filters/separation capabilities of Incinerator Type of



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burners: Fully automatic fuel oil burners. One each in primary and secondarychamber.

E) Fuel consumption: The operator should provide information on expected fuelconsumption.

F) Temperature attainable:1 Primary chamber: Minimum 850oC.2 Secondary chamber: Minimum Design Temperature Specified but shall

not be less than 1200 deg. C

In the secondary chamber gas residence time should be a least 1 or 2 sec. at 3%oxygen in the stack gas.

Material of construction:

1 Body: Fabricated from MS sheet.2 Lining: Both kiln and secondary combustion chamber to be lined with high

quality refractory and insulation.

3 Interlock system: Burners electrically interlocked while loading/unloadingwith micro switches.

4 Alarm: Audio visual alarm for all(i) Drive failures.

(ii) Excess temperature in PCC/SCC.

(iii) ID fan failure/FD fan failure.

(iv) Any other failure in the equipment, plant

G)Requirement of chimney:1 Height: Minimum 30 meters2 Material of chimney: Mild steel with rubber lining.3 Type: It shall be self supported having sampling point at appropriate place

of appropriate diameter along with ladder and platform for testing emissionlevel from chimney. Holes to be provided at distances as required forstandard method of testing.

H)Approx. life of Incinerator: - Shall not be less than 20 Years.I) The Operator shall have to furnish the expected minimum life of the Incinerator for

burning waste 720 TPA (Tonnes Per Annum) for moderate working of 24 hours/dayand a minimum of 300 days a year (App. expected life of Incinerator shall not be lessthan 20 years).

J) Combustion efficiency:



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Combustion efficiency (CE) should be at least 99.00%.

K) Approx. annual maintenance costThe approx annual maintenance cost shall be furnished with details of sparesgenerally required for continuous operation type Incinerator. The various aspects of

the scheduled maintenance required shall be highlighted with approximate cost.L) Emission Standards: (Maximum Value)

Suitably designed pollution control devices should be installed with theIncinerator so as to achieve emission levels given in the consent to establishmentissued by MPCB.

Effluent treatment plant should also be provided at the discharge point ofscrubbing medium. Final effluent should confirm to general standards foreffluents as per requirements under the law.

6.3.3.4 Details regarding installation and commissioningA)Type of installation preferred:

1 Under shed/indoor is preferred (developer shall have to supply all drawingsfor civil works).

2 Clear space area of approx. 10-12 meters shall be provided all around the unitfor smooth operation and maintenance.

3 Close walled waste collection area (dump yard shall be provided for keepingsolid waste).

B) Installation and commissioning: The developer shall install and commission theIncinerator at the BMWTSDF Site at Plot admeasuring.acre. in MUMBAIMaharashtra and has to give satisfactory demonstration to the concernedauthorities.

6.3.3.5 SafetyA)The Incinerator shall incorporate all safety devices so as to provide complete

protection to the developer and the unit against all possible operational/machineryfailures and these should be indicated clearly in the proposal.)



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7. TREATMENT STANDARDS/WASTE ACCEPTANCE CRITERIA FOR BMWTSDF7.1 IntroductionA)The treatment standards for the BMWTSDF are detailed in this section. The

standards are applicable during the term of the facility (i.e. 20 years). Theoverarching standards for the BMWTSDF would be as prescribed by CPCB, MoEFand MPCB authorisation and all standards in this section would be subservient tothese rules/guidelines. The standards detailed in this section relate to:-

Emission standards for Bio-medical Waste Incinerators as prescribed under The Bio-Medical Waste (Management and Handling) (Amendment) Rules 2003.

STANDARDS FOR INCINERATORS:

All incinerators shall meet the following operating and emission standards

A. Operating Standards

1. Combustion efficiency (CE) shall be at least 99.00%.

2. The Combustion efficiency is computed as follows:

%C02C.E. = ------------------ X 100

%C02 + % CO

3. The temperature of the primary chamber shall be 850 50 deg. C.

4. The secondary chamber gas residence time shall be at least I (one) second at1200 50 C, with minimum 3% Oxygen in the stack gas.

B. Emission Standards

Parameters Concentration mg/Nm3 at (12% CO2 correction)

(1) Particulate matter 150

(2) Nitrogen Oxides 450(3) HCL 50(4) Minimum stack height shall be 30 meters above ground(5) Volatile organic compounds in ash shall not be more than 0.01%

Note:



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Suitably designed pollution control devices should be installed/retrofittedwith the incinerator to achieve the above emission limits, if necessary.

Wastes to be incinerated shall not be chemically treated with any chlorinateddisinfectants.

Chlorinated plastics shall not be incinerated.

Toxic metals in incineration ash shall be limited within the regulatoryquantities as defined under the Hazardous Waste (Management and HandlingRules,) 1989.

Only low sulphur fuel like L.D.O/LS.H.S. /Diesel shall be used as fuel in theincinerator.

STANDARDS FOR WASTE STEAM STERILISATION

.

The autoclave should be dedicated for the purposes of sterilizing and treating bio-medical waste, to log 6 . Only regulated medical wastes such as bandages, gauges, vials,needles and syringes (if treatable), blood, body fluids and such pathological wastes(iftreatable shall be treated by this method)

(I) When operating a gravity flow autoclave, medical waste shall be subjected to:

(i) a temperature of not less than 121 C' and pressure of 15 pounds persquare inch (psi) for an autoclave residence time of not less than 60minutes; or

(ii) a temperature of not less than 135 C and a pressure of 31 psi for anautoclave residence time of not less than 45 minutes; or

(iii) a temperature of not less than 149 C and a pressure of 52 psi for anautoclave residence time of not less than 30 minutes.

(II) When operating a vacuum autoclave, medical waste shall be subjected to aminimum of one pre-vacuum pulse to purge the autoclave of all air. Thenecessary effluent treatment arrangement shall be provided to treat the purgedair to take care of evacuated airborne infected organisms. The waste shall be

subjected to the following:

(i) a temperature of not less than 121 C and pressure of 15 psi per anautoclave residence time of not less than 45 minutes; or

(ii) a temperature of not less than 135 C and a pressure of 31 psi for anautoclave residence time of not less than 30 minutes;



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(III) Medical waste shall not be considered properly treated unless the time,temperature and pressure indicators indicate that the required time, temperatureand pressure were reached during the autoclave process. If for any reasons, timetemperature or pressure indicator indicates that the required temperature,pressure or residence time was not reached, the entire load of medical waste

must be autoclaved again until the proper temperature, pressure and residencetime were achieved. The necessary documentary evidence shall be maintainedand submitted to regulatory authority by the operating agency of such repeatedsterilization procedure.

(IV) Recording of operational parameters

Each autoclave shall have graphic or computer recording devices, which willautomatically, and continuously monitor and record dates, time of day, loadidentification number and operating parameters throughout the entire length ofthe autoclave cycle. Any repeated sterilization cycles should be also

automatically reported.

(V) Validation test

Spore testing:

The autoclave should completely and consistently kill the approved biologicalindicator at the maximum design capacity of each autoclave unit. Biologicalindicator for autoclave shall be Bacillus stearothermophilus spores using vials orspore Strips; with at least 1X104 spores per milliliter. Under no circumstances willan autoclave have minimum operating parameters less than a residence time of

30 minutes, regardless of temperature and pressure, a temperature less than 121C or a pressure less than 15 psi.

(VI) Routine Test

Only spore testing will be acceptable. The spore vial should be placed at thecenter of the bagged waste or as recommended for the entire duration of thecycle and validated for 48 hours at the recommended CSSD department andlorin the validation unit provided by manufacturer. Such validation reports mustnecessarily be filed along with other records.

STANDARD FOR LIQUID WASTE: -The effluent generated from the hospital should conform to the following limits

PARAMETERS PERMISSIBLE LIMITS

pH 6.0 - 9.0Suspended solids 100 mg/lOil and grease 10 mg/l



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BOD 30 mg/lCOD 250 mg/lBioassay tests:- 90% survival of fish after 96 hours in 100% effluent.

These limits are applicable to those, hospitals, which are either connected withsewers without terminal sewage treatment plant or not connected to publicsewers. For discharge into public sewers with terminal facilities, the generalstandards as notified under the Environment (Protection) Act, 1986 should beapplicable.

STANDARDS OF MICROWAVING

1 Microwave treatment shall not be used for cytotoxic, hazardous or radioactivewastes, contaminated animal carcasses, body parts and large metal items.

2. The microwave system shall comply with the efficacy test/routine tests and aperformance guarantee may be provided by the supplier before operation of thelimit.

3. The microwave should completely and consistently kill the bacteria and otherpathogenic organisms that is ensured by approved biological indicator at themaximum design capacity of each microwave unit. Biological indicators formicrowave shall be Bacillus Subtitles spores using vials or spore strips with atleast 1 x 101 spores per milliliter.

SHREDDERA shredder to be used for shredding bio-medical waste shall conform to the

following minimum requirements:

1. The shredder for bio-medical waste shall be of robust design with minimummaintenance requirement.

2. The shredder should be properly designed and covered to avoid spillage and dustgeneration. It should be designed such that it has minimum manual handling.

3. The hopper and cutting chamber of the shredder should be so designed toaccommodate the waste bag full of bio-medical waste.

4. The design of shredder blade should be highly resistant and should be able to shredwaste sharps, syringes, scalpels, glass vials, blades, plastics, catheters, broken ampoules,intravenous sets/ bottles, blood bags, gloves, bandages etc. It should be able to handle/shred wet waste, especially after microwave/ autoclave/hydroclave.



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5. The shredder blade shall be of non-corrosive and hardened steel.

6. The shredder should be so designed and mounted so as not to generate high noise &vibration.

7. If hopper lid or door of collection box is opened, the shredder should stopautomatically for safety of operator.

8. In case of shock loading (non-shredable material in the hopper), there should be amechanism to automatically stop the shredder to avoid any emergency/accident.

9. In case of overload or jamming, the shredder should have mechanism of reversemotion of shaft to avoid any emergency/accident.

10.The motor shall be connected to the shredder shaft through a gear mechanism, toensure low rpm and safety.

11.The unit shall be suitably designed for operator safety, mechanical as well aselectrical.

12.The shredder should have low rotational speed (maximum 50 rpm). This will ensurebetter gripping and cutting of the bio-medical waste.

13.The discharge height (from discharge point to ground level) shall be sufficient(minimum 3 feet) to accommodate the containers for collection of shredded material.This would avoid spillage of shredded material.

14. The minimum capacity of the motor attached with the shredder shall be 3 kW for 50kg/hr, 5 kW for 100 kg/hr & 7.5 kW for 200 kg/hr and shall be three phase inductionmotor. This will ensure efficient cutting of the bio-medical wastes as prescribed in theBio-medical Waste (Management & Handling) Rules.

Sharp pit/ Encapsulation:

A sharp pit or a facility for sharp encapsulation shall be provided for treated sharps. Anoption may also be worked out for recovery of metal from sharps in a factory.

Vehicle/Container Washing Facility:

Every time a vehicle is unloaded, the vehicle and empty waste containers shall bewashed properly and disinfected. It can be carried out in an open area but on animpermeable surface and liquid effluent so generated shall be collected and treated inan effluent treatment plant. The impermeable area shall be of appropriate size so as toavoid spillage of liquid during washing.

Effluent Treatment Plant:



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A suitable Effluent Treatment Plant shall be installed to ensure that liquid effluentgenerated during the process of washing containers, vehicles, floors etc. is disposedafter treatment. The treated effluent shall comply with the stipulated regulatoryrequirements.

All the treatment equipment installed at the BMWTSDF shall comply with thestandards stipulated in the Bio-Medical Waste (Management & Handling) Rules, 1998.

7.2 NoiseA)Noise will be generated due to various sources namely:

1 Transportation to and within the area of the BMWTSDF.2 Loading and unloading activity inside the BMWTSDF.3 Diesel generating set and other power generating utilities in the BMWTSDF.4 Machinery/Equipment used inside the BMWTSDF, Dewatering, neutralisation,

pumps, boilers and Incinerator.

B) Standards to be achieved for day and night time shall be as per the following tablesspecified by CPCB guidelines. Noise standards for DG set shall be complied with asper norms prescribed by MPCB.

C) The Environmental (Protection) Rules 1986 - Standards in Respect of Noise are asfollows:

Area code Category of Area Limits in dB (A)

Day Time Night Time

1 Industrial Area 75 70

2 Commercial Area 65 55

3 Residential Area 55 45

4 Silence Zone 50 40

Note

1 Day time is reckoned in between 6 am and 9 pm2 Night time is reckoned in between 9 pm and 6 am3 Silence zone is defined as areas up to 100 meters around such premises as hospitals, educational institutions

and courts. The silence zones are to be declared by the Competent Authority.

4 Mixed categories of areas should be declared as one of the four above-mentioned categories by the CompetentAuthority and the corresponding standards shall apply

7.3 AestheticsA)Odour may get generated due to various sources such as:



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1 Volatilisation of organic constituents of wastes reaching the BMWTSDF andgetting exposed

2 Due to generation of gases during composting, anaerobic digestion and unduestorage of organic waste etc.

3 Conversion of chemicals or recovery of chemicals.B) The threshold odour values as specified under Environment (Protection) Act, 1986,

CPCB/MoEF guidelines and under the Rules framed under the Factory Act 1948amended in 1987 will have to be complied with.

C) The BMWTSDF operator will have to make proper segregation and transportation ofsuch wastes. There is no easy method to eliminate the odour and hence control atgeneration is essential. Oxidisation, camouflaging or dilution shall have to beadopted. MPCB authorisation may give a number of additional conditions and thesame will have to be addressed for e.g. tree plantations of appropriate pollutionindicator & pollution tolerant species.

7.4 Notification of compliance:The operator of the incinerator shall undertake comprehensive performance test. Within90 days of completion of comprehensive performance test, the operator shall issue anotification of compliance documenting compliance or non-compliance, as the case maybe, for public information.



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8.0 CRITERIA FOR SEGREGATION, COLLECTION & TRANSPORTATION

OF BIOMEDICAL WASTE

1. BACKGROUND:

Regulatory requirements for packaging, labeling, & transportation of Biomedicalwastes are given under Rule 6 of Biomedical Wastes (Management & Handling) Rules,1998, as amended 2003, notified under the Environment (Protection) Act, 1986. It is theresponsibility of the occupier or operator of a facility to ensure that Biomedical wastesare packaged, based on the composition in a manner suitable for handling, storage &transport. The labeling & packaging is required to be easily visible & be able towithstand physical conditions & climatic factors.

Without prejudice to the provisions under the Rule 6 of BMW Rules, 1998, as amended2003, & to further facilitate safe transportation of Biomedical wastes in compliance ofregulations, following guidelines are issued.

2. SEGREGATION AND COLLECTION:-

The medical waste shall not be mixed with other wastes. The medical waste shall be segregated into containers/bags at the point of

generation in accordance with schedule II prior to its storage, transportation,treatment and disposal.

Respective colored bags should be kept in similar colored container (colored bagsshall no be kept directly in vehicle)

Sharps shall be collected in puncture resistant containers. Temporary storage at healthcare unit shall be designated.

3. PACKAGING:

The containers when used for packaging of the Biomedical wastes should meetthe following requirements:

Composition of the wastes- the container should be compatible with thecharacteristics of the wastes e.g. acid-proof, leak proof etc.



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It should be waterproof. It shall have air vents, where applicable, to ensure that the gas generated does not

expand & deform / explode the container.

Container should be covered to minimum odor generation both at the point ofloading as well as during transportation.

Container should be easy to handle during transportation & emptying. As far as possible manual handling of containers should be minimized. Use

mechanical handling of containers should be considered.

Where 2-tier or 3-tier storage is envisaged the frame should have adequate strengthto hold the containers.

The containers should be washable & re-usable Design of the container should be such that it can be safely accommodated on the

transport vehicle. Dissimilar wastes shall not be collected in the same container. Wastes shall be

segregated & packed separately. This is necessary to ensure each waste finds its wayto right disposal pathway.

Occupier/ Biomedical waste generator shall not resort to the dilution of wastes(predominantly organic wastes)

Container shall be of mild steel with suitable corrosion resistance coating & roll onroll off cover which may either be handled by articulated crane or by a hook liftsystem works comfortably for a large variety of wastes. Other modes of packaging

like collection in 200 - L MS & plastic drums, card board cartons, PP & HDPE/LDPEcontainers also works for variety of wastes. However, all such container should beamenable to mechanical handling. The design & use of containers should be casespecific.

4. LABELING:

Labeling of containers is important for tracking the wastes from the point ofgeneration up to the final disposal. Following are the requirements for labeling:

Each container should be labeled according to schedule III of the Biomedical WasteRules, 1998, as mended 2003.

The label should contain the name & address of the waste management facilitywhere it is being sent for treatment & final disposal and also carry informationprescribed in schedule IV.

Emergency contact phone numbers shall be prominently displayed. For examplerespective Regional Officer of the State Pollution Control Board, Fire Station, PoliceStation.



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Label should include all relevant information as may required to facilitate safe andproper handling of Biomedical wastes.

It is in the interest of the operation to have named identification (on the ties or tapes)of each generator to enable definitive pin-pointing in case of error, negligence,whatever.

5. TRANSPORTATION:Following are the requirements pertaining to the transportation of Biomedical,

wastes.

Vehicle used for transportation shall be in accordance with the provisions under theMotor Vehicles Act, 1988, and rules made there under.

Untreated biomedical waste shall be transported only in such vehicle, as may beauthorized for the purpose by the competent authority as specified by theGovernment.

Transporter shall possess valid authorization from State Pollution Control Board fortransportation of wastes.

The vehicle shall be labeled with the bio-medical waste symbol (as per the ScheduleIII of the Rules) and should display the name, address and telephone number of theBMWTSDF.

PUCC (Pollution Under Control Certificate shall be properly displayed. Vehicle should be fitted with mechanical handling and transportation of the wastes. Name of the facility operator or the transporter, as the case may be, shall be

displayed.

Emergency phone numbers & TERM Card shall be displayed properly. Carrying of passengers & those working with the waste haulers shall be strictly

prohibited. Separate cabins shall be provided for driver/staff and the bio-medicalwaste containers.

Transporter shall carry documents of manifest during transportation as requiredunder the Rules.

The trucks shall be dedicated for transportation of Biomedical wastes & they shallnot be used for any other purpose. They should display BIOHAZARD sign.

Each vehicle shall carry first aid kit & fire extinguisher. Educational qualification for the driver shall be minimum of 10th pass (SSC).

Drivers shall be properly trained for handling the emergency situations & safetyaspects involved in the transportation of Biomedical wastes.



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The design of the trucks should be such that it should prevent spillage duringtransportation. They should slope towards idle to trap spillage with a small barriersto prevent outflow.

Transporter shall promptly attend pillages/accidents, if any, by providing suitableremedial actions as may be required.

Exposure of community to the odor, spillages & emissions from Biomedical wastesshall be avoided during transportation.

The base of the waste cabin shall be leak proof to avoid pilferage of liquid duringtransportation.

The waste cabin may be designed for storing waste containers in tiers. The waste cabin shall be so designed that it is easy to wash and disinfect. The inner surface of the waste cabin shall be made of smooth surface to minimize

Water retention.

The waste cabin shall have provisions of sufficient openings in the rear and/or sides so thatwaste containers can be easily loaded and unloaded.

6. STORAGE

(I) Sufficient ventilated storage space for untreated and treated bio-medical waste shall beprovided.

(II) The flooring and walls (to a height of 2M from floor) shall be finished with smooth andfine material. There shall be minimum number of joints.

7. RECORD KEEPING

(I) Every authorized person shall maintain records related to the generation, collection,

reception, storage, transportation, treatment, disposal and/or any form of handling of bio-medical

waste in accordance with these rules and any guidelines issued.

(II) All records shall be subject to inspection and verification by the prescribed authority atany time.

8. ANNUAL REPORT

Every occupier/operator shall submit an annual report to the prescribed authority inForm 11 by 31 January every year, to include information about the categories andquantities of bio-medical wastes handled during the preceding year. The prescribedauthority shall send this information in a compiled form to the Central PollutionControl Board by 31 March every year.



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9. ACCIDENT REPORTING

When any accident occurs at any institution or facility or any other site where bio-medical waste is handled or during transportation of such waste, the authorized personshall report the accident in Form Ill to the prescribed authority forthwith.



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SCHEDULE I

(See Rule 5)

CATEGORIES OF BIO-MEDICAL WASTE

------------------------------------------------------------------------------------------------------------------------Option Waste Category Treatment & Disposal------------------------------------------------------------------------------------------------------------------------Category No. I Human Anatomical Waste

(Human tissues, organs, body parts) incineration@/deep burial*

Category No. 2 Animal Waste(Animal tissues, organs, body parts carcasses, bleeding parts, fluid,incineration@/deep burial* blood and experimental animals used inresearch, waste generated by veterinary hospitals colleges, dischargefrom hospitals, animal houses)

Category No 3 Microbiology & Biotechnology Waste(Wastes from laboratory cultures, stocks or specimens of micro-localautoclaving/micro-organisms live or attenuated vaccines, human andanimal cell waving/incineration@ culture used in research andinfectious agents from research and industrial laboratories, wastesfrom production of biological, toxins, dishes and devices used fortransfer of cultures)

Category No 4 Waste sharps(Needles, syringes, scalpels, blades, glass, etc. that may causedisinfections (chemical treat-puncture and cuts. This includes bothused and unused sharps) ment@01/auto claving/micro-waving andmutilation/shredding"

Category No 5 Discarded Medicines and Cytotoxic drugs(Wastes comprising of outdated, contaminated and discarded inc-ineratio n@/destruct ion and medicines) drugs disposal in secured

landfills.

Category No 6 Solid Waste(Items contaminated with blood, and body fluids including cotton,dressings, soiled plaster casts, lines, beddings, other materialincineration@ contaminated with blood) autoclaving/micro waving



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Category No. 7 Solid Waste(Wastes generated from disposable items other than the waste sharpsdisinfections by chemical such as tubings, catheters, intravenous setsetc). Treatment @@ autoclaving/micro waving and

mutilation/shredding##

Category No. 8 Liquid Waste(waste generated from laboratory and washing, cleaning, house-disinfections by chemical keeping and disinfecting activities)treatment@@ and discharge

Category No. 9 Incineration Ash(ash from incineration of any bio-medical waste)disposal in municipallandfill

Category No. 10 Chemical Waste(Chemicals used in production of biological, chemicals used inchemical treatment@@ and disinfections, as insecticides, etc.)Dischargeinto drains for liquids and secured landfill for solids

------------------------------------------------------------------------------

------------------------------------------------------------------------------

@@ Chemicals treatment using at least 1% hypochlorite solution or any other equivalentchemical reagent. It must be ensured that chemical treatment ensures disinfections.

## Mutilations/shredding must be such so as to prevent unauthorized reuse.

@ There will be no chemical pretreatment before incineration. Chlorinated plastics shallnot be incinerated.

* Deep burial shall be an option available only in towns with population less than fivelakhs and in rural areas.

* These categories and suggested treatment are/should be subject to up gradation in 20year period.

So emphasis/weightage should be given to sterilization (log 6 upwards) and notdisinfection (log 4)



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SCHEDULE II

(See Rule 6)

COLOUR CODING AND TYPE OF CONTAINER FOR DISPOSAL OF BIO-MEDICAL WASTES

Colour

Conding

Type of Container -I Waste Category Treatment options as per

Schedule I

Incineration/deep burialYellow Plastic bag (non chlorinated/ bio degradable) Cat.1, Cat. 2, and Cat. 3,

Cat. 6.

Red Disinfected container/plastic bag (non chlorinated/bio degradable) Cat. 3, Cat. 6, Cat.7. Autoclaving/Microwaving/

Chemical Treatment

Blue/White

translucent

Plastic bag (non chlorinated/ bio degradable)

/puncture proof Cat. 4, Cat. 7.

Container

Autoclaving/Micro

waving/

Chemical Treatment and

Destruction/shredding

Black Plastic bag (non chlorinated/ bio degradable) Cat.

5 and Cat. 9 and

Cat. 10. (solid)

Disposal in secured

landfill

Notes:

1. Color coding of waste categories with multiple treatment options as defined in Schedule I,shall be selected depending on treatment option chosen, which shall be as specified in Schedule

I.

2. Waste collection bags for waste types needing incineration shall not be made of chlorinatedplastics.

3. Categories 8 and 10 (liquid) do not require containers/bags.

4. Category 3 if disinfected locally need not be put in containers/bags.

5. Weightage/preference will be given for least waste segregation requirement.



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SCHEDULE III

(See Rule 6)

LABEL FOR BIO-MEDICAL WASTE CONTAINERS/BAGS

HANDLE WITH CARE

Note: Label shall be non-washable and prominently visible.



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SCHEDULE IV

(See Rule 6)

LABEL FOR TRANSPORT OF BIO-MEDICAL WASTE

CONTAINERS/BAGS

Day ............ Month ..............Year ...........Date of generation ...................

Waste category No...Waste classWaste description

Sender's Name & Address Receiver's Name & Address

Phone No ........ Phone No ...............Telex No .... Telex No ...............Fax No ............... Fax No .................Contact Person ........ Contact Person .........

In case of emergency please contact

Name & Address:

Phone No.

Note:Label shall be non-washable and prominently visible.



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SCHEDULE VI

(See Rule 5)

SCHEDULE FOR WASTE TREATMENT FACILITIES LIKE INCINERATOR/

AUTOCLAVE/ MICROWAVE SYSTEM------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------A Hospitals and nursing homes in towns with population of 30 lakhs by 31st

December, 1999 or earlier and aboveB. Hospitals and nursing homes in towns with population of below

30 lakhs,(a) With 500 beds and above by 31st December, 1999 or earlier(b) With 200 beds and above but less than 500 beds by 31st December, 2000 orearlier

(c) With 50 beds and above but less than 200 beds by 31st December, 2001 orearlier(d) With less than 50 beds by 31st December, 2002 or earlier

C. All other institutions generating bio-medical waste not included by 31stDecember 2002 or earlier in A and B above

------------------------------------------------------------------------------

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FORM I

(See rule 8)

APPLICATION FOR AUTHORISATION

(To be submitted in duplicate.)

To

The Prescribed Authority(Name of the State Govt/UT Administration)Address.

1. Particulars of Applicant

(i) Name of the Applicant(In block letters & in full)

(ii) Name of the Institution:Address:Tele No., Fax No. Telex No./ Email address

2. Activity for which authorisation is sought:

(i) Generation(ii) Collection(iii) Reception(iv) Storage(v) Transportation

(vi) Treatment(vii) Disposal(viii) Any other form of handling

3. Please state whether applying for fresh authorisation or for renewal:(In case of renewal previous authorisation-number and date)

4. (i) Address of the institution handling bio-medical wastes:

(ii) Address of the place of the treatment facility:

(iii) Address of the place of disposal of the waste:5. (i) Mode of transportation (in any) of bio-medical waste:

(ii) Mode(s) of treatment:

6. Brief description of method of treatment and disposal (attach details):

7. (i) Category (see Schedule 1) of waste to be handled



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(ii) Quantity of waste (category-wise) to be handled per month

8. Declaration

I do hereby declare that the statements made and information given above is true tothe best of my knowledge and belief and that I have not concealed any information.

I do also hereby undertake to provide any further information sought by theprescribed authority in relation to these rules and to fulfill any conditions stipulated bythe prescribed authority.

Date: Signature of the Applicant

Place: Designation of the Applicant



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FORM II

(See rule 10)

ANNUAL REPORT

(To be submitted to the prescribed authority by 31 January every year).

1 . Particulars of the applicant:

(i) Name of the authorized person (occupier/operator):

(ii) Name of the institution:

Address

Tel. No

Telex No.

Fax No.

2. Categories of waste generated and quantity on a monthly average basis:

3. Brief details of the treatment facility:

In case of off-site facility:

(i) Name of the operator

(ii) Name and address of the facility:

Tel. No., Telex No., Fax No. , Email address

4. Category-wise quantity of waste treated:

5. Mode of treatment with details:

6. Any other information:

7. Certified that the above report is for the period from

Date ............................... Signature ...........................................

Place.............................. Designation..........................................



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FORM III

(See Rule 12)

ACCIDENT REPORTING

1. Date and time of accident:

2. Sequence of events leading to accident

3. The waste involved in accident:

4. Assessment of the effects of the accidents on human health and the environment,.

5. Emergency measures taken

6. Steps taken to alleviate the effects of accidents

7. Steps taken to prevent the recurrence of such an accident

Date ........... Signature..................

Place.................... Designation........................



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ANNEXURE-I

INFORMATION TO BE GIVEN TO BIDDERS

NUMBRER/DETAILONHOSPITALS, NURSING HOMES, CLINICS, DISPENSARIES,PATHOLOGY LABORATORY, BLOODBANKS, BIO-RESEARCHLABORATORIES,VETERINARY INSTITUTIONS, SLAUGHTER /ANIMALHOUSES



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ANNEXURE-II

PART LAYOUT PLAN OF MUMBAI AREA SHOWINGE W&CENTRAL ZONE BOUNDRIES

mpcb rfppart2

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