GMP


ASQ CertifiedcGMP Professional (1)
Equipment change in facility (3)
What is the responsibility of technical supervisor in production unit (2)
What action to be taken if an OOT result is confirmed (8)
Garment according to the clean room (3)
What is purpose of cross over bench in change room? (3)
What is glass policy please understand in briefly (6)
Equipment Gap Analysis and remediation plan (3)
Production environment in GMP WHO (1)
How to conduct audit in HEPA filter (3)
GMP guidelines for Active Pharmaceutical Ingredients (APIs) (2)
Mfg plant construction (1)
Production reworking (1)
GMP principals for hazardous drug manufacturing (1)
Expiry date for the raw materials (2)
GMP correction in executed documents (5)
Good documentation practices (1)
Paper shredder SOP (1)
How many HEPA filters will be placed in a clean room? and where it should be placed? (3)
Need to know data integrity part of SOP (1)
ICH Q7 Good Mfg practice API (2)
GMP certification (1)
Distance between Cephalosporin & general product plant (1)