Tags
pharmaceutical
ichq12
plcm
regulatory
compliance
gmp
q12
ich guideline
submission
post-approval variation
guideline
regulatory affairs
cmc
pacmp
product lifecycle management
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Presentations
(6)Likes
(6)PLCM - Categorisation - ICHQ12.pptx
GxPProfessional
•
1 year ago
Product Lifecycle Management Part 1 - ICHQ12.pptx
GxPProfessional
•
1 year ago
Data integrity in Pharmaceutical industry
GxPProfessional
•
3 years ago
ECDRP.pptx
GxPProfessional
•
1 year ago
NIMAR.pptx
GxPProfessional
•
1 year ago
MHRA manufacturing licence
GxPProfessional
•
1 year ago
Tags
pharmaceutical
ichq12
plcm
regulatory
compliance
gmp
q12
ich guideline
submission
post-approval variation
guideline
regulatory affairs
cmc
pacmp
product lifecycle management
variation
site master file
gdp
wda
distribution
medicine
special manufacturing
inspection
licence variation
manufacturing licence
mhra
data integrity
See more