Webinar on Implementing an Internal Audit Program of QMA, Persisting to ISO 13485 and 21 CFR Part 820

Description :
This webinar is intended to help you adequately develop an internal audit program of a firm's quality management system (QMS) as required by ISO 13485 or 21 CFR Part 820.
21 CFR 820.22 states "Each manufacturer shall establish procedures for quality audits and conduct such audits to assure that the quality system is in compliance with the established quality system requirements and to determine the effectiveness of the quality system."
This webinar will provide great opportunities to help you adequately establish your internal quality audit program with increased awareness and familiarity by employing risk- and process-based approaches pursuant to both ISO 13485 and 21 CFR 820.22.
At the end of the webinar, you will become familiar with the regulatory requirements for establishing an adequate internal audit program while bringing great benefits and added values to your firm's quality management system and contributing to saving an enormous amount of resources.
This webinar is a must to attend to ensure the adequacy of your internal audit program in conformity with the requirements set out in the ISO 13485 and 21 CFR 820.22.
Areas Covered in the Session :
Statutes and Regulations
Definitions
Comparative Overview of both ISO 13485 and 21 CFR Part 820
Auditing Strategy
Audit Objectives
Audit Planning, Frequency, Duration and Logistics
How to Audit Quality Management Systems
Various Audit Approaches
Quality Systems and Subsystems in ISO 13485
Quality Systems and Subsystems under 21 CFR Part 820
FDA and ISO 13485
Good Practices: Speaker’s Suggestions and Recommendations
Conclusion
Who Will Benefit:
Quality Professionals
Compliance Staff and Officers
Regulatory Affairs
Research & Development
Chief Executive Officers
Vice Presidents
Attorneys
Clinical Affairs
Consultants
Contractors/Subcontractors
Anyone Interested in the Topic for ISO 13485 or 21 CFR Part 820
Price tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299
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@compliancetrainings.com
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https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1510
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