Mots-clés
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
Tout plus
Présentations
(6)J’aime
(6)PLCM - Categorisation - ICHQ12.pptx
GxPProfessional
•
il y a 1 an
Product Lifecycle Management Part 1 - ICHQ12.pptx
GxPProfessional
•
il y a 1 an
Data integrity in Pharmaceutical industry
GxPProfessional
•
il y a 3 ans
ECDRP.pptx
GxPProfessional
•
il y a 1 an
NIMAR.pptx
GxPProfessional
•
il y a 1 an
MHRA manufacturing licence
GxPProfessional
•
il y a 1 an
Mots-clés
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
Tout plus