Netzealous LLC DBA - Compliance4All, Online
2018-12-07
Overview: This webinar will help you understand the FDA's current thinking on computer systems that are validated and subject to inspection and audit.
Areas Covered in the Session: 21 CFR Part 11, Electronic Records/Electronic Signatures (ER/ES) Data Archival to ensure security, integrity and compliance Validation Strategy that will take into account the system risk assessment and system categorization (GAMP V) processes Recent FDA findings for companies in regulated industries
Who Will Benefit: Anyone who is involved in the development, testing, manufacturing, storage, handling and distribution of product must understand and conform to FDA requirements for data quality and integrity, and computer system validation (CSV) Finally, anyone who is acting as a consultant or contractor to a company in an FDA-regulated industry should attend to ensure they are able to bring the most current knowledge and expertise to their assignment
Event Fee: One Dial-in One Attendee Price: US$290.00
Contact Detail: Compliance4All DBA NetZealous, Phone: +1-800-447-9407 Email: support@compliance4All.com
|