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2016 - Webinar on Internal Auditing
Date2016-02-04
Deadline2016-02-04
VenueOnline, Canada 
KeywordsInternal Auditing; Documentation requirements; CAPA
Topics/Call fo Papers
Description :
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 Covered in the Session :
SOP and documentation requirements
Training requirements
Audit schedules
Carrying out audits
Audit responses
CAPAs for Internal audits
Who Will Benefit:
Quality Control Teams
Quality Assurance Teams
Production Teams
Purchasing Teams
Operations Teams
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 Covered in the Session :
SOP and documentation requirements
Training requirements
Audit schedules
Carrying out audits
Audit responses
CAPAs for Internal audits
Who Will Benefit:
Quality Control Teams
Quality Assurance Teams
Production Teams
Purchasing Teams
Operations Teams
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Last modified: 2016-01-13 19:57:28