This webinar will explain the basic principles of Internal Auditing in the pharmaceutical and medical device industries. Particular emphasis will be the specific requirements set out in 21 CFR Part 210/211/820 and how these requirements can be met.
You will learn the current industry standards for creating and maintaining Internal audit systems.
Areas to be Covered:
SOP and documentation requirements
Carrying out audits
CAPAs for Internal audits
Who will Benefit:
Quality Control Teams
Quality Assurance Teams