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good manufacturing practices for finished pharmaceuticals (21 CFR 211)
cGMP Training: Deviation handling is important area to reporting and investigation & documentati...
About pharmacy
A brief presentation on the current good manufacturing practices employed in the manufacture of phar...
Code of federal regulations
Documentation is an integral part of good manufacturing practices. It defines a system of informatio...
Presented By :- Raghav Sharma Class :- M.Pharm, 1st sem. Department :- Pharmaceutics Institute :- Pa...
job ordering and costing is basic course in accounting and business. it will help to have detail an...
ich guidelines
Use of QA and QC in Pharmaceutical Industries
SUPAC respresents the changes recommended by US FDA at the time of scale up or approval of NDA / AND...
Technology transfer in pharmaceutical industry
Pilot plant scale up techniques
Rasa ratna samuchchaya have dedicated a separate chapter for rasashala which can be corelated to GMP...
drug master file and distribution record of drug in pharmaceutical industry and its types
cosmetic, regulatory provision, schedule M, condition of licence, schedule U, prohibition of certain...
validation in pharmacy
Pharmacy
DETAILING ABOUT THE TRANSACTION
Inspection report
GMP,GLP,USFDA, etc