21 CFR Part 11 and Annex 11 Compliance - Specifics Needed to Eliminate 483s

This 21 CFR Part 11 compliance training will guide you through the requirements of Part 11 and will also explain its 3 primary areas: SOPs, product features and validation (10 step risk based approach).

Why Should You Attend:

This webinar will describe exactly what is required for compliance with Part 11 and the updated European equivalent Annex 11. It will take the concepts described in the regulations and expand them into specifics for all three primary compliance areas: SOPs, product features, and validation.

Who Will Benefit:

Computer system users

IT personnel

QA personnel

Managers

Executives

Instructor Profile:

Computer System Validation’s principal, David Nettleton, is an industry leader, author, and instructor on topics pertaining to 21 CFR Part 11, Annex 11, HIPAA, software validation, and computer system validation. His wide knowledge on these subjects comes from his involvement in the development, purchase, installation, operation, and maintenance of computerized systems used in FDA compliant applications.

Note:

Use coupon code NB5SQH8N and get 10% off on registration, Valid till Dec 31st 2015.

For Registration:

http://www.complianceonline.com/fda-21-cfr-part-11-compliance-requirements-computer-system-validation-webinar-training-701687-prdw?channel=sciencedz