2016 - Webinar on Deviations and Investigations

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
For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada
Customer Support : #416-915-4458
Email : support-AT-compliancetrainings.com
For more information about this event please visit
https://compliancetrainings.com/SiteEngine/Product...