Good Documentation Practices to Support FDA Computer System Validation at 26468 E Walker Dr, Aurora

Location 26468 E Walker Dr, Aurora, Colorado 80016-6104, Aurora, Colorado, 80016
Event Date(s) Thursday November 2, 2017
Prices $199.00
Event Website Visit Event Website >
Event Category Business/Networking, Business Events

OVERVIEW This webinar will leave you with the information needed to create and maintain good documentation that meets FDA compliance standards. You will learn about what must be done and what must not be done. In addition, you’ll learn about the various computer system validation deliverables and how to document them. FDA requires that all documentation related to GxP products GMP, GLC, and GCP) be created and maintained in accordance with specific rules. From the color of the ink used to the retention requirements, you’ll learn all about how to create and maintain good FDA-compliant documentation. WHY SHOULD YOU ATTEND You should attend this FDA regulatory compliance training if you are responsible for any FDA-regulated data and/or records. All documents need to be created and maintained in accordance with FDA guidelines for good documentation to avoid any issues during an inspection or audit. You will also benefit from learning about the guidelines for computer system validation and the many deliverable documents that need to be produced in a way that is FDA-compliant. Having completed this course, you will be on your way to successful future FDA audits and inspections. AREAS COVERED • FDA Good Documentation Practices • Computer System Validation CSV) • System Development Life Cycle SDLC) Methodology • GAMPV System Categorization • Industry Best Practices • Potential Pitfalls WHO WILL BENEFIT • Information Technology Analysts • QC/QA Managers • QC/QA Analysts • Clinical Data Managers • Clinical Data Scientists • Analytical Chemists • Compliance Managers • Laboratory Managers • Automation Analysts • Computer System Validation Specialists • GMP Training Specialists • Business Stakeholders responsible for computer system validation planning, ution, reporting, compliance, maintenance and audit • Consultants working in the life sciences industry who are involved in computer system implementation, validation and compliance • Auditors engaged in the internal inspection of labeling records and practices All FDA-regulated industries: • Pharmaceutical • Biological • Medical Device • Tobacco LEARNING OBJECTIVES • To understand how to create, revise and maintain documentation that is FDA-regulated. • To understand the many deliverables required to complete a computer system validation effort. • To understand industry best practices. • To understand and avoid potential pitfalls. For more detail please click on this below link: https://goo.gl/NCV7DV Email: support@trainingdoyens.com Toll Free: +1-888-300-8494 Tel: +1-720-996-1616 Fax: +1-888-909-1882


Bizarre & Unusual  |  Concerts & Festivals  |  Entertainment & Themed Events  |  Expos, Trade Shows & Fairs  |  Family & Kids  |  Gay & Lesbian
International Events  |  Literature & Books  |  Motorsports  |  Shopping & Fashion  |  Social & Hobby  |  Special Events & Holiday Parties  |  Sporting Events  |  Theater & Arts  | 
About  |  Contact Us  |  Popular Searches  |  Testimonials  |  Useful Links  |  Newsletter  |  Bookmark  |  Terms of Use  |  Privacy Policy  |  Log In

Copyright © 2017 Chooseyourevent.com Inc. 2300 N. Barrington Road - Suite 400, Hoffman Estates, IL 60169. All rights reserved