SOP on Good Laboratory Practices as per schedule L1
Good laboratory practices need to be performed in the laboratory for consistent, reliable analytical results. This SOP introducing about Good …
SOP on Change Control Note, Role of Change Control Board
This SOP is introducing what is change control system, what is the change control board, what is the procedure of change …
SOP on Good Documentation Practices
Introducing SOP on Good Documentation Practices (GDP). All pharmaceutical industry follows the good documentation practices for the consistency in documentation. …
SOP on Annual Product Quality Review (APQR) and How to Prepare Standard Format for APQR/APR
SOP for Annual product quality review (APQR/APR/PPR/PQR) which is the best tool in pharmaceuticals for identification of the process/method consistency, the …
PPT of Current Good Manufacturing Practices (cGMP)
PPT/ Powerpoint presentation of current Good Manufacturing Practices (cGMP), GMP, the content of PPT is what is cGMP, the definition …
SOP on Site Master File (SMF) and How to prepare Site Master File as per guideline
Standard operating procedure on Site Master File (SMF) is describes, What is a site master file and what are the requirements of the …
What is the risk and How to minimize the risk of TSE (Transmissible Spongiform Encephalopathy) / BSE (Bovine Spongiform Encephalopathy)
What is Transmissible Spongiform Encephalopathy (TSE) / Bovine Spongiform Encephalopathy (BSE). How to minimize the risk of TSE/BSE in pharmaceuticals. …