Address the Paradigm Shift in Regulatory Inspections

Jun 28, 2018

Register Free: http://www.chromatographyonline.com/lcgc_w/inspections

The term “FDA audit” can trigger many responses, including dread and panic. It also raises many questions. What triggers a regulatory audit? How has the FDA changed its auditing strategy and what are they focused on? What systems are likely to get inspected? In addition to answering these questions, this webcast will focus on ensuring data integrity in an analytical laboratory. Join us to learn from Humera Khaja, Agilent’s software compliance expert with nearly a decade of regulated software experience.

 

Speakers:

Humera Khaja, Software Compliance Program Manager, Informatics Division, Agilent Technologies

 

Date and Time:

Live: Thursday, 28 June, 2018 | North America: 1 pm EDT | Europe: 1900 CEST

After the final airing of the webcast on 28 June, 2018 it will be available on demand until 28 June, 2019. 

Sponsor: Agilent Technologies, Inc.

Register Free: http://www.chromatographyonline.com/lcgc_w/inspections

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