Browsing Tag
Regulatory affairs
157 posts
EU regulations for manufacture and sale of nutraceuticals. PPT
EU regulations for manufacture and sale of nutraceuticals www.DuloMix.com1 1. European Union Directives andRegulations for manufactureand sale…
Drug and Medical device product failures and the stability of the pharmaceutical supply Chain. PPT
Drug and Medical device product failures and the stability of the pharmaceutical supply Chain Department of Drug Regulatory…
The EU system for marketing/ European Union & Australia PPT
Chapter 2European Union & Australia College of Pharmacy The EU system for marketing authorization (MA) www.DuloMix.com 2…
Regulatory requirement for drug product approval .US and Canada / PPT
Regulatory requirement fordrug product approval: US and Canada College of Pharmacy USFDA www.DuloMix.com 2 Background •…
the approximation of the laws of the Member States relating to food supplements. 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 PRODUCT. PDF
GUIDELINES ON GOOD DISTRIBUTION PRACTICES FOR BIOLOGICAL PRODUCTS Document No : CDSCO/GDP.BP Ver. : 00 Effective…
IMDRF Introduction PDF/PPT
IMDRF Introduction IMDRF is a voluntary group of medical device regulators from around the world who have come…
global device nomenclature PDF/PPT
The global device nomenclature refers to the standardized naming conventions and classification systems used to identify and categorize…
Six steps to CE marking 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 PDF/PPT
BRAZIL, ASEAN, CIS, AND GCC COUNTRIES 1 ASIAN Countries a. Introduction to ACTD b. Regulatory Requirement for registration…