Electronic Records & Electronic Signatures; 21 CFR Part 11 2013
14 Mar 2013
Webinar
Description
Topics
General Provisions
History and Overview
Electronic Signatures
Electronic Records
Scope & Application Guidance
Who should Attend
Quality Assurance staff
Project/Strategic Management
Operations staff
IT staff
Staff members from companies which may develop software or computer systems for FDA regulated companies
Staff members from FDA regulated companies involved in Validation of those systems, Computerized system projects or maintenance/security of electronic records
Past Events
Electronic Records & Electronic Signatures; 21 CFR Part 11 2013 - 14 Mar 2013, Webinar (36715)
Important
Please, check "Electronic Records & Electronic Signatures; 21 CFR Part 11" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Pharma
Industry: Food & Beverages
Technology: Biotechnology, Data management, Information Technology (IT)