Good Documentation Practices to Support FDA Computer System Validation

Date : 11th February 2020 to 11th February 2020

Place : United States, Aurora

Website :http://bit.ly/36Hyoqu

Contact Person:Training Doyens

Description:

Learn good documentation practices for FDA regulated documents and records, and computer system validation guidelines to ensure that your procedures meet the FDA compliance standards.

Good Documentation Practices to Support FDA Computer System Validation will be held in Aurora,United States on date 2020-02-11

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Deadline for abstracts/proposals : 11th February 2020

Keynote Speakers : Years of Experience: 35+ years Areas of Expertise: Strategic Planning, Project Management, FDA Regulatory Compliance, Organizational Development & Effectiveness, and Change Leadership & Management Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health and other FDA-regulated industries. She is currently managing a large, complex data migration, analytics and reporting program at a major financial insti

Conference Highlights :OVERVIEW FDA requires that all documentation related to GxP products (GMP, GLC, 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. The 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 a

Venue :26468 E Walker Dr, Aurora, Colorado 80016, USA

Check the event website for more details.