Webinar On Computer System Validation

4 March 2015, Mississauga, Canada


Introduction
Computer System Validation is a regulatory requirement under ICH GCP and 21 CFR Part 11 but it also makes good business sense to ensure that computerized systems will perform consistently as expected. Validation of Computerized Systems has a very specific set of tasks that are often mismanaged, resulting in missed deadlines, increased costs, and regulatory risk, and missed times to market for a company’s product. Achieving the validated state requires much more than just User Acceptance Testing. This detailed webinar will explain the basic tenets of of 21 CFR 11 compliance for Computer Systems Validation and will show how to deliver on time and on budget while meeting regulatory compliance requirements in a more effective manner.
Areas Covered in the Session :
How big is computer system validation?
Regulatory background and useful definitions
The validation process
The importance of documentation
User Acceptance Testing (UAT)
Maintaining the validated state
Who Will Benefit:
This webinar is a must for:
Regulatory Affairs Staff
Data Managers
Clinical Affairs Staff
Clinical Research Professionals
Monitors
Programmers
Statisticians
Any company that uses a computerized system to give input to new systems specifications and/or User Acceptance Testing
Price tags:
Live
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Recording
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299

Speakers
Venue
Online

Compliance Trainings, Online, 5939 Candlebrook Ct, Ontario, Mississauga, L5V 2V5, Canada

Organised by
Compliance Trainings
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