natar rapid test booklet 26may2016 · email: [email protected] website: iso-9001: 2008 13485...

Bringing the

RAPIDTESTTECHNOLOGYto New & Dynamic Brilliance

NPW : Nectar Polytechnic for Women Social Activities Employee Welfare

Unit I (D) WHO - GMP Sterile Cephalosporin APIs./Intermediates

Unit II (D) Corporate QA/QC/ RA/ R&D blockOC: Ce�xime Trihydrate*OD: Cefuroxime Axetil Crys* OE: Multiproduct Plant*OG : Cefuroxime Axetil Amph* Utilities block : Steam, Power & Water

Unit III (D) CONTRACT MANUFACTURING Plant

Unit IV (D) Solvent Recovery Plant

Unit V (D) Green Technology Power generation plant

Unit VI (B) Cephalosporin Finished Dosage Forms - Oral & Injectables

Unit VII (B) Empty Hard Gelatin Capsules

Unit VIII (J) Phyto-chemicals manufacturing Unit - I

Unit IX (D) Phyto-chemicals manufacturing Unit - II

Unit X (D) Phyto-chemicals manufacturing Unit - III

Unit XI (D) Sterile Cephalosporin facility - APIs (D & E Block)

Unit XII (D) Diagnostic manufacturing plant

Unit XIII (L) Guargum plant

Manufacturing Facilities

USFDA CE EUGMP WHO cGMP Globally EHS compliant

ISO 9001:2008 ISO 13485 ISO 22000 : 2005 ISO 14001 : 2004 ISO 50001

OHSAS 18001 : 2007 KOSHER HALAL C-14 SA 8000 : 2008

Sustainability

Accreditation

Social Accountability System-SA 8000 : 2008 Certi�ed

Nectar Lifesciences Ltd.SCO 38-39, Sector 9-D Chandigarh-160 009, IndiaTel.: +91-172-3047777, 3078158Fax: +91-172-3047755

Nectar Lifesciences USA LLC500 Oberlin AvenueLakewood, NJ 08701United States

Nectar Lifesciences UK Ltd. Devonshire House60, Goswell RoadLondon- EC1M 7AD

New Jersey(USA)

UK (London)

HQ-Chandigarh

Nectar Lifesciences Ltd.Website: www.neclife.comEmail: [email protected] ISO-9001: 200813485

INDEX

Bio-fuel Based CaptivePOWER GENERATION PLANTNectar produces 18MW electricity through cogeneration which has a net positive impact on both environment and quality of life of the local population. It is a zero discharge & eco friendly facility. This reduces energy bill, has minimum transmission, distribution losses & has no burden on government power generation and ensure 24 Hrs. uninterrupted power supply for our company.

1. Pregnancy (hCG) Test ........................................................................................................1

2. Ovulation (LH) Test ..........................................................................................................2

3. Malaria (P.f. / P.v.) Antibody Test......................................................................................3

4. Malaria (P.f. / P.v.) Antigen Test ......................................................................................4

5. Hepatitis B (HBsAg) Test ..................................................................................................5

6. Hepatitis C (HCV) Test ......................................................................................................6

7. HIV 1/2 Rapid Test ............................................................................................................7

8. HIV 1/2/0 Rapid Test..........................................................................................................8

9. Dengue NS 1 Rapid Test....................................................................................................9

10. Troponin I Test (Cardiac Marker) ..................................................................................10

11. Syphilis (VDRL) Test ......................................................................................................11

12. Upcoming Products ......................................................................................................12

13. Clinical Chemistry Reagents .................................................................................. 13-15

Nectar Lifesciences Ltd.

Nectar Lifesciences is an Indian integrated pharmaceutical organisation with leadership in cephalosporin antibiotics Active pharmaceutical ingredients, �nished dosage forms, diagnostic products, empty hard gelatin capsules and agricultural products such as menthol derivatives.

Nectar started its operations in 1997 and now Its annual revenue exceeds 300 million USD. About Nectar:

• India's top 300 organization; Business World, INC

• India's top 20 Pharmaceutical organization; Business World, Fortune 500

• Public company listed on BSE and NSE; Reuters NECT.BO

• Dun & Bradstreet D-U-N-S' 86-237-2356

• Financial rating A

• 13 Manufacturing facilities spread over 400,000 sq m

• 2000+ employees

• 37 USDMFs �led and more than 15 ANDAs

• 28 patents; R&D with more than 100 scientists

• Exports to over 50 countries

• Star Trading House (Government of India)

PROFILE

BUSINESS AREASLIFESCIENCES

1. Pharmaceutical • Active Pharmaceutical Ingredients • Finished dosage forms

2. Empty hard gelatin capsules

3. Consumer Healthcare

4. Diagnostic and Surgicals • In vitro diagnostics • Patient care • Home health Products • RAPID TEST & REAGENTS

NATURAL PRODUCTS

1. Menthol and mentha derivatives

2. Guar gum powder

NECTAR LIFESCIENCES LTD.

PREGNANCY (hCG) TEST

Product Description

For the rapid determination of human chorionic gonadotropin (hCG) in urine. This test is used to obtain a visual qualitative result for pregnancy.

Pack Size: 1x30 Tests (Large Casette) 1X50 Tests (Small Casette)

Components: • Test Device • Dropper • Package Insert

InformationHuman chorionic gonadotropin (hCG) is a glycoprotein hormone secreted by the developing placenta shortly after fertilization. In normal pregnancy hCG can be detected in serum as early as 7 days following conception, dubling every 1.3 to 2 days and reading 100mlU/ml at the first missed menstrual period. One step pregnancy test device is a qualitative, sandwich dye conjugate immunoassay for the determination of human hCG in urine. The method employs a unique combination of monoclonal and polyclonal antibodies to selectively identify hCG in test sample with high degree of sensitivity.

Interpretation

1 32Positive: Two lines appear. One coloured line should be in the control line region (C) and another apparent coloured line should be in the test line region (T).

Negative: One coloured line appears in the control line region(C). No line appears in the test line region (T).

Invalid: No visible band at all or test band without control band.

Draw 2-3 drops of urine sampleinto the sample dropper1 Read the result within 10 minutes. (Time

varies depending on hcg concentration)3Dispense it into the sample wellon the test device2

Procedure

Pack Size: 1x5 Tests


OVULATION (LH) TEST

Visit our Website www.pregaplan.com to know more about Pregaplan.

Interpretation


Negative: One coloured line appears in the control line region(C). No line appears in the test line region (T) or faint line appears in the test line region.


Product Description

Pregaplan is an Ovulation device to check if a female is ovulating. Pregaplan One -Step Ovulation test is a rapid chromatographic immunoassay for detecting the luteinizing hormone (LH) in urine, as an aid for the early detection of ovulation.

InformationOvulation is the release of an egg from the ovary. The egg passes into the fallopian tube where it is ready to be fertilized. In order for pregnancy to occur, the egg must be fertilized by sperm within 24 hours after its release. Immediately prior to ovulation, the body produces a large amount of luteinizing hormone (LH). Pregaplan Test Device detects human luteinizing hormone through visual interpretation of color development on the device. It is a complete system to help you predict the time of ovulation and peak fertility. It is during this fertile time that pregnancy is most likely to occur. Pregaplan Ovulation Test Device detects the LH surge in urine, signaling that ovulation is likely to occur in the next 24-36 hours.

Draw 3 drops of urine sampleinto the sample dropper1 Read the result within 10 minutes.

Do not interpret results after 15 minutes.3Dispense it into the sample wellon the test device2

Procedure

1 2

ISO-9001: 200813485

ISO-9001: 200813485

MALARIA (P.f. / P.v.) ANTIGEN TEST


Components: • Test Device • Chase buffer • Package Insert • Dropper

Product Description

One Step Malaria P.f. / P.v. whole blood antigen Test is a rapid, qualitative determination of Malaria antigen in human blood as an aid for in vitro diagnosis of Malaria infection

InformationMalaria remains one of the most serious tropical and subtropical diseases in many countries of the world. It is rampant in most areas of the tropics. One step malaria Pf/Pv antigen Test contains a membrane strip, which is pre-coated with two monoclonal antibodies as two separate lines across a test strip. One monoclonal antibody (test line 1) is specific to the P. falciparum histidine rich protein -2 (pf HRP II ) and another monoclonal antibody (test line 2) is pan specific to lactate Dehydrogenase (Pan LDH) of plasmodium species (P.Falciparum,Vivax,Malariae,Ovale).

Interpretation

1 32Positive: The presence of two color bands (C and 1) indicates a positive result for P. falciparum. The presence of two color bands (C and 2) indicates a positive result for P. Vivax. The presence of 3 colored bands indicate a positive result for P falciparum and P Vivax

Negative: One coloured line appears in the control line region(C). Invalid: No visible band at all or test band

without control band.

Add 5µl of whole blood into sample well("S" sample well)1 Read the test result at 20 mins3Add 2 drops or 60-80 µl of Chase buffer

into buffer well2

Procedure

MALARIA (P.f. / P.v.) ANTIBODY TEST

Product Description

One Step Malaria P.f. / P.v. antibody Test is a rapid self – performing, qualitative determination of Malaria antibodies in human blood as an aid for in vitro diagnosis of Malaria infection

InformationMalaria is casued by a parasite that is transmitted from one person to person by the bite of infected Anopheles mosquitoes. One Step Malaria P.f. / P.v. antibody Test is an immunochromatographic (rapid) test for the qualitative detection of antibodies of all isotopes (IgG,IgM,IgA) specific to Plasmodium falciparum and Plasmodium vivax simultaneously in human serum, plasma or whole blood. Test contains a membrane stripe, pre-coated with recombinant malaria Pf capture antigen (MSP, CSP) on test band 1 region and with recombinant malaria Pv antigen (MSP, CSP) on test band 2 region.

Interpretation

1 32Positive: The presence of two color band (“1”and “C”) indicates a positive result for infection with P. falciparum.The presence of two color bands (“2” and “C”) indicates a positive result for infection with P. vivax.The presence of three color bands (“T1”, “T2” and “C”) indicates a positive result for “mixed” infection.

Negative: One coloured line appears in the control line region(C). No line appears in the test line region (T)



Components: • Test Device • Chase buffer • Package Insert • Dropper

Add 10 µl (one drop) of serum / plasma or20 µl (two drops) of whole blood to thesample well(S) 1 Interpret test results in 10 to 20 minutes.

Do not read results after 30 minutes.3Add 2 drops of clearing buffer2

Procedure

ISO-9001: 200813485

ISO-9001: 200813485

3 4

ONE STEP MALARIA P.F. / P.V. ANTIGEN TEST ONE STEP MALARIA P.F. / P.V. ANTIBODY TEST

4

HEPATITIS B (HBsAg) TEST

Product Description

One step hepatitis B surface antigen test (Australian antigen test) Device (Serum/Plasma) is a rapid chromatographic Immunoassay for the qualitative detection of Hepatitis B surface Antigen in serum or plasma.

InformationHepatitis B is transmitted sexually or intravenously and has an incubation period of six months. If not diagnosed properly and in time, it can develop in to acute or chronic infection, liver cirrhosis and fulminant hepatitis. The test method uses monoclonal antibody conjugated to colloidal gold and polyclonal antibody immobilized on a nitrocellulose strip in a thin line. If the sample contains HBsAg, the colloidal gold-antibody (mouse) conjugate binds to the antigen forming an antigen antibody-colloidal gold complex. The complexes then migrate through the nitrocellulose strip by capillary action which is stopped by an immobilized antibody zone forming a color band.

Interpretation






Add 2 drops of serum or plasma to the specimen well witha disposable dropper.1 2 Read results before 20 minutes. Strong positive reaction may

visible within 5 minutes.

Procedure

Interpretation




Product Description

The HCV One Step Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of antibody to Hepatitis C Virus in serum or plasma.

InformationHepatitis C is an infectious disease caused by the hepatitis C virus (HCV) that primarily affects the liver.The HCV One Step Rapid Test is a lateral flow chromatographic immunoassay based on the principle of the double antigen–sandwich technique. The membrane is coated with recombinant HCV antigen on the test line region of the device. During testing, the serum or plasma specimen reacts with the HCV antigen coated particles.Presence of this coloured line indicates a positive Result.

HEPATITIS C (HCV) TEST


Components: • Test Device • Package Insert • Buffer • Dropper

Procedure

Add 1 drop of serum or plasma intothe sample window using provideddisposable dropper1 Read results within 15 Minutes.

(Do not interpret the result after 20 minutes.)3Add 2 drops (60-70µl) of buffer2

ISO-9001: 200813485

ISO-9001: 200813485

5 6

HIV 1/2 RAPID TEST


Components: • Test Device • Buffer • Package Insert • Dropper

Interpretation




Product Description

The HIV I & II Rapid Human Immunodeficiency Virus Test (Serum/Plasma) is a rapid immunoassay for the qualitative detection of Human Immunodeficiency Virus (HIV) type-1 and/or type-2 in serum or plasma. Test contains single test line for detection of HIV 1 or HIV 2.

InformationHIV is the etiologic agent of Acquired Immuno Deficiency Syndrome (AIDS). Testing human serum or plasma for the presence of HIV antibodies has proven an effective aid in determining whether an individual has been exposed to HIV. The HIV I & II Rapid Human Immunodeficiency Virus Test (Serum/Plasma) is a lateral flow chromatographic immunoassay based on the principle of the double antigen–sandwich technique. The membrane is coated with recombinant HIV recombinant antigens on the test line region of the device. When a specimen is applied at one end of the membrane, it reacts with HIV recombinant antigen coated gold conjugate in the test. If the serum or plasma contains antibodies to HIV-1 or HIV-2, a colored line will appear in the test line region, showing a positive result.

Add 1 drop of serum or plasma intothe sample window using provideddisposable dropper1 Read results within 15 Minutes.


Procedure

ISO-9001: 200813485

HIV 1/2/0 RAPID TEST

Product Description

The HIV Triline, Rapid Human Immunodeficiency Virus Test (Serum/Plasma) is a rapid immunoassay for the qualitative detection of Human Immunodeficiency Virus (HIV) type-1 and/or type-2 separately.

InformationThe HIV Triline (1/2/0) Rapid Human Immunodeficiency Virus Test is a lateral flow chromatographic immunoassay based on the principle of the double antigen–sandwich technique. The membrane is coated with recombinant HIV 1 and HIV 2 recombinant antigens in the test line region 1 and 2 of the device. When a specimen is applied at one end of the membrane, it reacts with HIV recombinant antigen coated gold conjugate in the test. The mixture then migrates chromatographically by capillary action and reacts with the recombinant HIV recombinant antigens on the membrane in the test line region. If the specimen contains antibodies to HIV-1 or HIV-2, a colored line will appear in the test line region 1 & 2, showing a positive result.

Interpretation

1 32Positive: Two or three lines appear. One colored line should be in the control line region (C) and another apparent colored line should be test region 1 or 2 or both (1 & 2 printed on the test device)





Add 1 drop of serum or plasma into thesample window using provided disposabledropper1 Read results within 15 Minutes.


Procedure

7 8

ISO-9001: 200813485

TROPONIN I TEST (CARDIAC MARKER)

Product Description

The Troponin I Rapid Test Device is a rapid visual immunoassay for the detection of cardiac Troponin I in human whole blood, serum, or plasma specimens. This kit is intended to be used as an aid in the diagnosis of myocardial infarction (MI).

InformationAfter cardiac injury occurs, Troponin I is released into the blood 4-6 hours after the onset of pain.Troponin I remains elevated for 6-10 days, thus providing for a longer window of detection for cardiac injury.The Troponin I Rapid Test Device has been designed to detect cardiac Troponin I through visual interpretation of color development in the strip. The membrane is immobilized with anti-cTnI antibodies on the test region. During the test, the specimen is allowed to react with colored anti-cTnI antibodies colloidal gold conjugates, which are precoated on the sample pad of the test. The mixture then moves on the membrane by a capillary action, and interact with reagents onthe membrane. If there are enough cTnI in specimens, a colored band will form at the test region of the membrane. Presence of this colored band indicates a positive result.

Pack Size: 1x30 Tests 1x1 Test (Monocarton)


Interpretation




1Add two drops of serum or plasma into the sample window using provided disposable dropper

3 4For Fingerstick Whole Blood: Allow 1 hanging drop of fingerstick whole blood specimen to fall into the center of the specimen well (S), then add 2 drops of buffer

Wait for the colored band(s) to appear. The result should be read at 20 minutes.

2For Venipuncture Whole Blood specimens: Add 2 drops of whole blood to the specimen well (S), then add 1 drop of buffer

Procedure

Product Description

The Dengue NS1 Antigen Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of dengue virus NS1 antigen in whole Blood, serum or plasma to aid in the diagnosis of Dengue viral infection.

InformationDengue viruses, transmitted by the Aedes aegypti and Aedes albopictus mosquitoes, are widely distributed throughout the tropical and subtropical areas of the world.The Dengue NS1 Antigen Rapid Test is a qualitative membrane strip based immunoassay for the detection of dengue virus NS1 antigen in Whole Blood /Serum / Plasma. In this test procedure, anti-Dengue NS1 antibody is immobilized in the test line region of the device. After a Whole Blood/Serum/Plasma specimen is placed in the specimen well, it reacts with anti-Dengue NS1 antibody coated particles that have been applied to the specimen pad. If the specimen contains dengue virus NS1 antigen, a colored line will appear in the test line region indicating a positive result.

DENGUE NS 1 RAPID TEST

Interpretation




Pack Size: 1x30 Tests 1x1 Test (Monocarton)



3 4For Fingerstick Whole Blood: Allow 2 hanging drops of fingerstick whole blood specimen to fall into the center of the specimen well (S), then add 1 drop of buffer


2For Venipuncture Whole Blood specimens: Add 2 drops of whole blood to the specimen well (S), then add 1 drop of buffer

Procedure

9 10

ISO-9001: 200813485

ISO-9001: 200813485

UPCOMING PRODUCTSSYPHILIS (VDRL) TEST

Product Description

The Syphilis Ultra Rapid Test Device is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Treponema Pallidum (TP) in whole blood, serum or plasma to aid in the diagnosis of Syphilis.

InformationSyphilis is a sexually transmitted infection caused by the bacterium Treponema pallidum subspecies pallidum.The Syphilis Ultra Rapid Test Device (Whole Blood/Serum/Plasma) is a qualitative membrane device based immunoassay for the detection of TP antibodies (IgG and IgM) in whole blood, serum or plasma. In this test procedure, recombinant Syphilis antigen is immobilized in the test line region of the device. After a specimen is added to the specimen well of the device, it reacts with Syphilis antigen coated particles in the test. This mixture migrates chromatographically along the length of the test strip and interacts with the immobilized Syphilis antigen. The double antigen test format can detect both IgG and IgM in specimens. If the specimen contains TP antibodies, a colored line will appear in the test line region, indicating a positive result.



Interpretation





3 4For Fingerstick Whole Blood: Allow 1 hanging drop of fingerstick whole blood specimen to fall into the center of the specimen well (S), then add 2 drops of buffer


2For Venipuncture Whole Blood specimens: Add 1 drop (20µl) of whole blood to the specimen well (S), then add 2 drops of buffer

Procedure

ZIKA IgG/IgM VIRUSANTIGEN

RAPID TEST

CHIKUNGUNYA IgMRAPID TEST DEVICE

RAPID TEST FORDRUGS OF ABUSE

TYPHOID RAPID TEST

KALA AZAR RAPID TEST

HEPATITIS A VIRUSRAPID TEST

DENGUE NS1IgG/IgM COMBO

11 12

ISO-9001: 200813485

CLINICAL CHEMISTRY REAGENTS

PRODUCT METHODOLOGY PACK SIZE

TOTAL PROTEIN BIURET METHOD 2X100ML

TOTAL PROTEIN (BIURET) BIURET METHOD 1X 100 ML

UREA BERTHLOT END POINT 2X50ML

UREA UV (FS) UV KINETIC GLDH 1X100ML

URIC ACID (FS) URICASE-PAP 5X22ML

URIC ACID (FS) URICASE-PAP 2X22ML

KIDNEY PROFILE

GLUCOSE LYPHOZ GOD-POD METHOD 5X100ML

GLUCOSE MONO (FS) GOD-POD METHOD 2X500ML

GLUCOSE MONO (FS) GOD-POD METHOD 5X100ML

GLUCOSE GOD/POD METHOD 4X50 ML

GLUCOSE GOD/POD METHOD 9X50 ML

DIABETIC MONITORING

CALCIUM ARSENAZO ARSENAZO METHOD 5X22ML

CALCIUM OCPC OCPC 2X25ML

LG CALCIUM TEST KIT OCPC 2X 50 ML

CHLORIDE THIOCYNATE METHOD 1X25ML

CHLORIDE TEST KIT THIOCYNATE 100 ML

PHOSPHORUS (FS) MOLYBDATE METHODS 1X25ML

PHOSPHORUS UV MOLYBDATE MOLYBDATE METHODS 1X 50 ML

ELECTROLYTES

WIDAL SLIDE (WITH ANTIGEN O & H) AGGLUTINATION 2+2X5ML

WIDAL SLIDE (WITH DIFFERENT COLORED ANTIGENS) AGGLUTINATION 4X5ML

SEROLOGY

ASO TURBI TURBIALTEX 45+5 ML

CRP TURBI TURBIALTEX 45+5 ML

RF TURBI TURBIALTEX 45+5 ML

TURBILATEX



ALK.PHOSPHATASE (FS) AMP BUFFER & IFCC KINETIC 5X10ML

ALP TEST KIT PNPP AMP BUFFER & IFCC KINETIC 10X5 ML

SGOT(AST) (FS) IFCC KINETIC 100ML

SGPT(ALT) (FS) IFCC KINETIC 100ML

SGPT (ALT) IFCC UV KINETIC 10X10 ML

SGOT( AST) IFCC UV KINETIC 10X10 ML

TOTAL & DIRECT BILIRUBIN DMSO METHOD 2X100ML

T&D BILIRUBIN TEST KIT (J&G) DMSO METHOD 2X 125 ML

LIVER PROFILE

CHOLESTEROL (FS) CHOD-POD METHOD 5X22ML

CHOLESTEROL CHOD-POD METHOD 2X20 ML



HDL-CHOL DIRECT DIRECT TEST 1X20ML

LDL-CHOL DIRECT DIRECT TEST 1X20ML

TRIGLYCERIDES KIT (FS ) GPO-PAP METHOD 5X22ML

TRIGLYCERIDES KIT (FS) GPO-PAP METHOD 2X22ML

TRIGLYCERIDES TEST KIT (GPO/TRI) GPO-PAP METHOD 2X 50 ML

LIPID PROFILE

ALBUMIN BCG METHOD 5X52ML

ALBUMIN BCG METHOD 1X 100 ML

AMYLASE (FS) CNPG2 METHOD 2X10 ML

AMYLASE (CNPG3) CNPG2 METHOD 1X5 ML

CREATININE ALK. PICRATE METHOD 4X50ML

CREATININE (JAFFS REAGENT) PICRATE METHOD 2X50 ML

HEMOGLOBIN DR (FS) CYANOMETHEMOGLOBIN 1000ML

MICROPROTEIN PYAROGALLOL METHOD 2X22ML

MICROPROTEIN TEST KIT PG.RED PYAROGALLOL METHOD 1X 25 ML

KIDNEY PROFILE

13 14

ISO-9001: 200813485

ISO-9001: 200813485



PRODUCT SPECIFICATION PACK SIZE

ASO LATEX LATEX AGGLUTINATION 25T

ASO LATEX LATEX AGGLUTINATION 50T

CRP LATEX LATEX AGGLUTINATION 25T

CRP LATEX LATEX AGGLUTINATION 50T

RF LATEX LATEX AGGLUTINATION 25T

RF LATEX LATEX AGGLUTINATION 50T

LATEX RANGE

LYTIC SOLUTION FOR 3/5 PART HEMATOLOGY ANALYZER 1LTR.

DETERGENT (RINSE) FOR 3/5 PART HEMATOLOGY ANALYZER 1 LTR. / 5 LTR.

DILUENT FOR 3/5 PART HEMATOLOGY ANALYZER 10 LTR. / 20 LTR.

HEMATOLOGY REAGENTS

OUR CEO MR. DINESH DUA RECEIVING

PHARMEXIL GOLD AWARD

OUR MD MR. SANJIV GOYAL RECEIVING

NATIONAL ENERGY CONSERVATION AWARD FROM

POWER MINISTER OF INDIA

15

Our facility is situated 250 kms north of New

Delhi, India, in the foothills of the

Himalaya mountains. The closest airport is in

the beautiful city of CHANDIGARH

(Airport code - IXC), which is 30 minutes

away from our facility.Chandigarh, being the

capital city of the states of Punjab and Haryana, is well connected by air and rail to major cities

of India.

ISO-9001: 200813485

natar rapid test booklet 26may2016 · email: [email protected] website: iso-9001: 2008 13485...

Documents