Good Documentation Practice (GDocP) for FDA Regulated Industries

Website https://worldcomplianceseminars.com/upcoming_webinar | Edit Freely

Category Quality Control/Quality Assurance, Regulatory Affair, Laboratory, Manufacturing

Deadline: January 23, 2020 | Date: January 23, 2020

Venue/Country: Online Webinar, U.S.A

Updated: 2020-01-04 14:46:49 (GMT+9)

Call For Papers - CFP

Documentation is the key to GMP compliance and ensures traceability of all development, manufacturing, and testing activities.

This good documentation practice webinar will discuss how to secure, manage and govern your documentation in compliance with GxP/GMP requirements and be able to pass quality audit. Also attendees will learn the connection between CxP/GMP and document control and more..,

Session Highlights:

• GxP/GMP and Documentation

• Purpose of Document Control

• Controlled Documents – Types, Identification

• Role of QA in Document Control

• Document Control Procedures

• Document Management System

• Measuring Success of Document Control System

• Change Control Procedure

Speaker:

Galaxy Consulting Founder and President Eleonora Babayants has many years of GxP/GMP hands-on experience in regulated industries. She worked with quality assurance and compliance officers to develop and execute compliance strategies and programs. She participated in the implementation of compliance requirements.