Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance

This webinar on validating legacy computer systems will give a good understanding of FDA and EU regulatory requirements for validation (retrospective validation) and provide tools for effective implementation.

Why Should You Attend:

When existing or legacy computer systems are used in FDA or equivalent international environments they should be validated, a process sometimes called retrospective validation. While the industry is very well familiar with the validation of new systems, there are many questions about existing or legacy systems.

This web seminar will give a good understanding on the regulatory requirements, and it will have recommendations and provide tools for effective implementation.

Hand-Outs:

For easy implementation, attendees will receive

• SOP: Retrospective Validation of Computerized Systems
• Checklist: Retrospective Validation of Computer Systems

Note: These complimentary hand-outs will be sent to customers on request. Please emailcustomercare@complianceonline.com for these documents, stating your order number, and they will be emailed to you within 4 working days.

Who will Benefit:

• IT managers and system administrators
• QA managers and personnel
• QC and Lab managers
• Validation specialists
• Regulatory affairs
• Training departments
• Documentation department
• Consultants