medical devices regulation reforms in india - who · medical devices regulation reforms in india...
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Medical Devices
Regulation reforms
in
india
Dr. S. eswara reddy
Joint Drugs Controller, CDSCO (HQ)
11th May 2017 , Generva
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Basic Concept
Drug ________To__________Device
Harmonised regulation
Best Practices fallowed in other Countries
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Medical Devices Rules 2017
Published on 31st January 2017
Effective from 01-01-2018
Classification
MD Grouping
Essential Principle for manufacturing
Product Standards
Regulatory Reforms
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Regulatory Reforms Notified Bodies
Registration
Medical Device Officer
Qualification
MD Testing Officer
Central MD Testing Laboratories
Established or designated
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Online application
Class A & B... By State Government
Inspection by Notified body
Class C & D....by Central Government
Perpetual validity of license
Suspension/Cancellation....on Websites
Test License by CLA
Environmental conditions for manufacturing
MD Rules ...Manufacturing
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Only import license
All classes of devices
Perpetual validity of license
GHTF countries in Rules – Rely on other countries
If not approved in GHTF, Clinical Investigation
Post approval changes...Major / Minor
Recall provision
Materiovigillanve
MD Rules ...Import
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Labelling
Local Market
Export
Unique Device Identification of MD
Registration of Laboratories
Export Certificate
Rejection of application.....Misleading, Fake,
Fabrication
Debarment of application
MD Rules ...Miscellaneous
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Requirements for approval of product
Regulatory Compliance Class A Class B Class C Class D
QMS
Electrical Safety/EMI/EMC testing
data * * * *
Risk Analysis Report
Device Master File
Biocompatibility data ** ** **
Animal Testing ** **
Clinical Data *** ***
* Only for Electrical supply based devices **Only for invasive or implantable devices ***Only for Investigational devices 8
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Materiovigilance Programme of India(MvPI)
Materiovigilance Program of India
(MvPI) has been launched by DCG (I)
on 6th July 2015 at Indian
Pharmacopoeia Commission (IPC)
Ghaziabad.
IPC Ghaziabad functions as National
Coordination Centre for MvPI.
Sree Chitra Tirunal Institute
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“Pharmacovigilance” is one of the core functions in the
WHO global NRA benchmarking tool
The WHO NRA re-benchmarking exercise, from 13-17
February 2017, was aimed at assessing the status of the India
vaccine regulatory system
Assessment of the National Regulatory
Authority (NRA) of India
Ensuring quality, safety and efficacy of vaccines
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