- TypeWebinar
- Location Fremont, California, United States
- Date 15-04-2020
Education/Teaching/Training/Development
Business Development
Medical/Healthcare/Hospital
OTHERS
Overview:
This webinar describes the validation planning process with particular emphasis on avoiding six common pitfalls.
Increased use of software from automated manufacturing and quality systems means increased exposure. Most recalls can be traced back to computerized equipment, exposing the validation process to scrutiny. Corporate uncertainty leads to inaction and "wheel spinning." Many companies struggle with understanding how to avoid major mistakes when validating software to FDA standards.
Why you should Attend: Avoid the 6 most common problem associated with Part 11 and Annex 11 compliance. Learn how to efficiently create the specific documents required to implement data integrity requirements.
Areas Covered in the Session:
Who Will Benefit:
Speaker Profile
David Nettleton, is an FDA Compliance Specialist for 21 CFR Part 11, HIPAA, and Computer System Validation. His latest book is "Risk Based Software Validation - Ten easy Steps" that relates to the development, purchase, installation, operation and maintenance of computerized systems used in regulated applications. He specializes in performing gap analysis, remediation plans, SOP development, vendor audits, training, and project management. He has completed more than 185 mission critical software validation projects.
Event link:
https://www.compliance4all.com/webinar/--502974LIVE?channel=bioalps-APR_2020_SEO
Contact Info
Netzealous LLC, DBA -Compliance4all
Email: [email protected]
Phone: +1-800-447-9407
Website: https://www.compliance4all.com/
39658 Mission Boulevard, Fremont, CA 94539, USA.
8004479407 Fax No: 94539