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Quality assurance audits in pharma industries
rasika walunj
•
8 years ago
REGULATORY REQUIREMENTS FOR ASEAN COUNTRIES
Vikas Rathee
•
4 years ago
Pms
Sayeda Salma S.A.
•
6 years ago
The Unique Device Identification System for Class I and Unclassified Devices
EMMAIntl
•
4 years ago
Medical Devices: EU Directives, Guidance Documents, CE Marking Process and ISO Certification Programs
ComplianceOnline
•
13 years ago
Rule 11 and imdrf ue 2017 745 v06
Antonio Bartolozzi
•
4 years ago
Novel foods
EFSA EU
•
7 years ago
EU Food Regulation on Additives, Novel Foods and Food Contact Materials
Daniele Pisanello
•
7 years ago
China: Medical Device Regulations
Pacific Bridge Medical
•
10 years ago
Biologics ppt
Tanujacappi
•
4 years ago
Drug approval process in japan
Manish kumar
•
7 years ago
ACTD- ASEAN
Naila Kanwal
•
8 years ago
ICH-GCP Guidelines
Abel C. Mathew
•
4 years ago
USFDA guidelines of glp for non clinical testing laboratories
swrk
•
10 years ago
Pharmacy act
Chandrika Mourya
•
4 years ago
NARCOTIC DRUG AND PSYCHOTROPIC SUBSTANCE ACT 1985 AND RULES
DeepikshaSahu1
•
3 years ago
THE NARCOTIC DRUGS AND PSYCHOTROPIC SUBSTANCESACT 1985 (NDPS ACT)
PuttaChandraLekha
•
4 years ago
The Prevention of cruelty to animals act 1960
Rajveer Bhaskar
•
8 years ago
Cdsco Roles and Responsibilities
Sandip Mavchi
•
4 years ago
Bio-equivalence study of drugs
pharmacampus
•
2 years ago