Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820 2014
09 Apr 2014
Webinar
Key Topics
ISO 13485
Statutes and Regulations
Auditing Strategy
Definitions
Audit Planning, Frequency, Duration and Logistics
Audit Objectives
Various Audit Approaches
How to Audit Quality Management Systems
Quality Systems and Subsystems under 21 CFR Part 820
Quality Systems and Subsystems in ISO 13485
FDA and ISO 13485
Comparative Overview of both ISO 13485 and 21 CFR Part 820
Good Practices: Speaker’s Suggestions and Recommendations
Who should Attend
Compliance Staff and Officers
Quality Professionals
R&D
Regulatory Affairs
VPs
CEOs
Clinical Affairs
Attorneys
Contractors/Subcontractors
Consultants
Anyone Interested in the Topic for ISO 13485 or 21 CFR Part 820
Past Events
Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820 2014 - 09 Apr 2014, Webinar (43829)
Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820 2026
Important
Please, check "Establishing an Internal Audit Program of the Quality Management Systems Pursuant to ISO 13485 and 21 CFR Part 820" official website for possible changes, before making any traveling arrangements
