Webinar On Computerized System Validation: Basic Concepts

MessageThis Webinar is over
Date Feb 24, 2015
Time 13:00 pm
Cost $249.00
Description :
The basic concepts of computerized system validation originated in the 1960s, with the Department of Defense and NASA. Validation of systems became a growing issue within the pharmaceutical industry during the late 1980s and early 1990s, as the use computerized technologies became commonplace in the research and manufacturing of drug products. The FDA issued a series of regulations and guidelines to define regulatory expectations for computerized system validation. In today’s pharmaceutical environment, virtually all aspects of research and manufacturing are conducted using computerized systems, yet the planning, conduct, and necessary controls for validation of these systems remains problematic for many companies and industry professionals.

Recommended webinar for FDA regulated companies, any staff members who may be involved with computerized system validation project planning, validation testing, system use, system support, and regulatory compliance of computerized systems.

Areas Covered in the Session :
Introduction, Historical Perspective, and Definitions
Computerized System Validation Master Plan
Validation Plan
Developer Assessment
Requirements, Design, and Configuration Specifications
Validation Testing
Validation Summary Report
Commissioning Memo
System Decommissioning/Retirement
Questions & Answers

Who Will Benefit:
 Professionals who will benefit are:
Project Management
Strategic Management
Quality Assurance staff
IT staff
Operations staff

Price Tags:
Single Live : For One Participant
$ 249
Corporate Live : For Max. 10 Participants
$ 899
Single REC : For One Participant - Unlimited Access for 6 Months
$ 299

For more information and enquiries contact us at
Compliance Trainings
5939 Candlebrook Ct, Mississauga, ON L5V 2V5, Canada 
Customer Support : #416-915-4458 
Email : support@compliancetrainings.com

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