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Regulatory Affairs
Webinar
Feb. 15, 2023
–
Feb. 15, 2023
Advanced Compliance Writing CAPA: Mastering Failure Investigation and Root Cause Analysis
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Webinar
Feb. 16, 2023
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Feb. 16, 2023
Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success
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Webinar
Feb. 22, 2023
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Feb. 22, 2023
Best Practices for Developing and Maintaining a GxP Training Matrix
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Webinar
Mar. 07, 2023
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Mar. 07, 2023
FDA’s Remote Assessments v. Remote Interactive Evaluations: Do You Really Know the Difference?
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Upcoming Events
08
Feb
Process and Design Validation for Devicemakers: A Deep Dive into Best Practices, Recent Trends and Regulatory Definitions
09
Feb
The Inextricable Link Between Data Integrity and Quality Culture
15
Feb
Advanced Compliance Writing CAPA: Mastering Failure Investigation and Root Cause Analysis
16
Feb
Fundamentals of FDA Inspection Management: Reduce Anxiety, Increase Inspection Success
22
Feb
Best Practices for Developing and Maintaining a GxP Training Matrix
07
Mar
FDA’s Remote Assessments v. Remote Interactive Evaluations: Do You Really Know the Difference?
Featured Products
FDA’s New Quality System Regulation: Transitioning from QSR to ISO 13485
Selecting and Implementing Electronic Document Management Systems in the EU
Featured Stories
FDA Updates Smiths Medical CADD System Recall to Class I
Eisai’s New Alzheimer’s Drug Leqembi Hits the U.S. Market
Boston Scientific’s Single Use Ureteroscope Gets FDA Clearance
Gilead’s Trodelvy Gets Expanded Approval in Breast Cancer
The Revised ICH E8:
A Guide to New Clinical Trial Requirements
Learn More