MAY 03

Computer Systems Validation


All other Events(no CPF)




  03 May 2018 through 03 May 2018


  Online Event

Website URL:

Sponsoring organization:

  Training Doyens


  Medicine & Health > Pharmaceutical/Medicinal

Event description:

OVERVIEW This will cover the history of Computer Systems Validation in the Pharmaceutical and Medical Device industries. This led to the regulation 21 CFR Part 11, which covers the management of both electronic signatures and electronic records. Compliance to relevant regulations using Standard Operating Procedures and required documentation will be covered. The roles of Audits, Quality Assurance, and Risk Management will also be covered. WHY SHOULD YOU ATTEND Changes continue to be implemented in many existing computer systems and in many cases computer systems are being replaced or upgraded using new technologies. Many of these changes require Validation and Validation typically involves almost everyone who uses or supports the systems. Doing Validation is a “Project” that requires participation of many of those involved in the system. Some of this involves strong management commitment to the accuracy and quality of the products of the systems. AREAS COVERED • History of Validation Regulations • Some CSV Standards to use • Standard Operating Procedures • Necessary Documentation LEARNING OBJECTIVES • Understand Computer Systems Validation • Cover The role of Electronic Records • Learn the Compliance to 21 CFR Part 11 • The role of Qualification in Validation • Preparation of Standard Operating Procedures • The Documentation needed for Validation WHO WILL BENEFIT • IT Staff • Computer System Users • Quality Assurance • Regulatory • System Vendors For more detail please click on this below link: Email: Toll Free: +1-888-300-8494 Tel: +1-720-996-1616 Fax: +1-888-909-1882

Posting date:

12 April 2018
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