Does Your Electronic Data System Meet 21 CFR Part 11 and CGMP Requirements?

Register free: http://www.chromatographyonline.com/lcgc_w/electornic_data_system

Event Overview:

Does your electronic data system meet 21 CFR Part 11 and CGMP requirements? And, how is it achieved? The answer is through data integrity and data security.

Your regulated analytical laboratory must maintain the integrity of electronic data by understanding where and how your data systems log information throughout the data life cycle. This includes data generation and recording (data acquisition); transformation and collection (interpretation and data analysis); reporting, review and archiving.

In this interactive webcast, Humera Khaja, Global Software Compliance Program Manager in the Life Sciences & Applied Markets Group at Agilent Technologies, will explore critical areas that enable data integrity for better regulatory compliance in each step of your analytical workflow.

Key Learning Objectives:

• Understand the key aspects of your e-workflow in relation to your business processes

• Understand what technical controls exist in your software and how they affect data integrity

• Understand your audit trails and logs: Can you explain them? How do you find out what triggered an error?

Speaker: Humera Khaja, Global Software Compliance Program Manager, Agilent Technologies, Inc.

Time and date: Thursday, Jul. 25, 2019 | North America: 9am EDT | Europe: 3pm CEST | India: 6:30pm IST

On demand available after airing until Jul. 25, 2020.

Sponsor: Agilent Technologies, Inc.

Register free: http://www.chromatographyonline.com/lcgc_w/electornic_data_system