This webinar will explain the basic principles of Deviations and Investigations 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.
In this webinar you will learn the current industry standards for carrying out and documenting deviations and investigations.
Areas Covered in the Session :
SOP and documentation requirements
Carrying out investigations
Who Will Benefit:
Quality Control Teams
Quality Assurance Teams