How is this differs from 21 CFR Part 820?
Part 820 applies to medical device manufacturers. (referred to as QSR or cGMP) and Part 211 applies to pharmaceutical companies. (referred to as cGMP)
What is the Purpose of cGMP for pharmaceuticals?
Define the regulations for the minimum current good manufacturing practice for preparation of drug products for [...] Read more »
21 CFR Part 211 in Easy-to-Understand Terms
SundayDec 21,2008
What is Difference between Validation and Verification in Software Testing?
SundayDec 21,2008
Verification is done by frequent evaluation and meetings to appraise the documents, policy, code, requirements, and specifications. This is done with the checklists, walk throughs, and inspection meetings.
Different activities are carried out to ensure that we are building the product right. Activities like Peer reviews , Inspections , code walk-thru’s, Audits.
Verification is done [...] Read more »