GOVERNMENT & REGULATORY BODIES IN THE WORLD
GMP REGULATIONS
USFDA
21 CFR PART 11
21 CFR PART 58
21 CFR PART 110
21 CFR PART 111
21 CFR PART 210
21 CFR PART 211
21 CFR PART 600
21 CFR PART 601
21 CFR PART 606
21 CFR PART 610
21 CFR PART 700
21 CFR PART 701
21 CFR PART 820
GUIDANCE LIST- HUMAN DRUGS
GUIDANCE LIST - BIOLOGICS
GUIDE TO INSPECTION
USFDA 483s & Warning Letters
WHO GMP
EMA
EU GMP- EUDRALEX VOLUME 4
EUDRALEX VOLUME 3
ICH Q7 GMP FOR APIs
INDIAN CDSCO GMP- SCHEDULE M
CHINA SFDA GMP
JAPAN PMDA GMP
AUSTRALIA TGA GMP
GUIDES FROM OTHER ORGANIZATIONS
IPEC GUIDES- EXCIPIENTS
APIC PUBLICATIONS
ISPE GAMP GUIDES
ISPE TECHNICAL GUIDES
PDA TECHNICAL REPORTS
ISO STANDARDS
ICH GUIDELINES
PIC/S GMP GUIDE
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SEETHARAM KANDARPA
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