Browsing Tag
Regulatory affairs
157 posts
DIRECTIVE 2002/46/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 10 June 2002 PPT/PDF
12.7.2002 EN Official Journal of the European Communities L 183/51 DIRECTIVE 2002/46/EC OF THE EUROPEAN PARLIAMENT AND OF…
GUIDELINES ON GOOD DISTRIBUTION PRACTICES FOR BIOLOGICAL PRODUCTS PPT/PDF
GUIDELINES ON GOOD DISTRIBUTION PRACTICES FOR BIOLOGICAL PRODUCTS Document No : CDSCO/GDP.BP Ver. : 00 Effective…
IMDRF Introduction PPT/PDF
IMDRF Introduction IMDRF is a voluntary group of medical device regulators from around the world who have come…
GMDN stands for Global Medical Device Nomenclature PPT/PDF
GMDN stands for Global Medical Device Nomenclature. It’s a system used to identify and classify medical devices internationally.…
The Canadian Trade Commissioner Service Everywhere you do business PPT/PDF
The Canadian TradeCommissioner ServiceEverywhere you do business A Canadian Trade Commissioner Service White Papertradecommissioner.gc.ca Six steps to CE…
BRAZIL, ASEAN, CIS, AND GCC COUNTRIES PPT/PDF
BRAZIL, ASEAN, CIS, AND GCC COUNTRIES 1 ASIAN Countries a. Introduction to ACTD b. Regulatory Requirement for registration…
EMERGING MARKET ▪ Class : M.Pharm (Department of Regulatory Affair) PPT/PDF
EMERGING MARKET ▪ Class : M.Pharm(Department of Regulatory Affair) www.DuloMix.com 1 EMERGING MARKET ➢ An emerging market…
EMERGING MARKET ➢ Introduction : PPT/PDF
EMERGING MARKET ➢ Introduction : An emerging market (or an emerging country or an emerging economy) is a…
PRODUCT LIFE CYCLE FOR MEDICAL DEVICES PPT/PDF
The product life cycle for medical devices typically includes five stages:Development: This stage involves research, design, and prototyping…
ORGANIZATION OF PMDA PPT/PDF
ORGANIZATION OF PMDA PMDA (Pharmaceuticals and Medical Devices Agency) is Japanese regulatory agency, working together with Ministry of…