Compliance Trainings, Online
2016-03-11
Description : 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 Training requirements Carrying out investigations Deviation tracking Who Will Benefit: Quality Control Teams Quality Assurance Teams Production Teams Purchasing Teams Operations Teams
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