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2016 - Webinar on Deviations and Investigations
Date2016-03-11
Deadline2016-03-11
VenueOnline, Canada 
KeywordsFDA Investigations; FDA Deviations; Documentation requirements
Topics/Call fo Papers
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
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
Other CFPs
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- Webinar on Corrective and Preventive Action (CAPA) utilizing the Principles of Lean Documents and Lean Configuration
- Webinar on Computer System Validation
- Webinar on FDA Quality Metrics and Risk Based Inspections
Last modified: 2016-01-13 19:49:28