Slide 1 Good Documentation Practice The 1972 Devonport, UK, incident resulted in at least five deaths when drug products designed to be sterile became contaminated and recipients…
This is a presentation that I developed and gave to the GMP constituency of a medium-sized biopharmaceutical company to satisfy one of the requirements for ongoing cGMP training.…
Good Manufacturing Practices (GMP) for Pharmaceutical Excipients Guided by presented by k.Shantha kumari MAM p.sambasiva rao M.Pharm,Ph.D y12mph0864 I/IIM.PHARMACY NIRMALA…
1 VALIDATION BOOT CAMP LIFECYCLE APPROACH TO PHARMACEUTICAL VALIDATION – PRINCIPLES, IMPLEMENTATION, AND PRACTICE Paul L. Pluta, PhD Journal of Validation Technology Journal…
A SUMMER TRAINING & PROJECT REPORT ON “PREVAILING SCENARIO OF INDUSTRIAL REALTIONS AT SANOFI AVENTIS PHARMA” AT (SANOFI AVENTIS PHARMA) SUBMITTED TO: SHRI R R TANTI…