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Home
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Events
» Postmarket Safety
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Archives
Postmarket Safety
Webinar
EU-MDR: Are You Ready? An Exclusive Three-Part FDAnews Webinar Series
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Data Integrity in the COVID-19 Era and Beyond: A Three-Part FDAnews/CenterWatch Virtual Conference Series
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Webinar
May 24, 2022
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May 24, 2022
Quality Culture: You Can’t Improve What You Don’t Measure — Practical, Innovative Diagnostic Tool Allows Companies to Measure and Improve Their Quality Culture
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Webinar
Jun. 09, 2022
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Jun. 09, 2022
How to Standardize your Lab Investigation Process: Increase Efficiency and Reduce Risk with a Consistent Process
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Webinar
Jun. 21, 2022
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Jun. 21, 2022
Medical Device Reporting: Best Practices and Common Pitfalls
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Webinar
Jun. 22, 2022
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Jun. 22, 2022
Meet CDRH’s New Strategic Priorities: Where the Center is Headed and How Devicemakers Can Keep Up
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Virtual Workshop
Jun. 28, 2022
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Jun. 30, 2022
Effective Root Cause Analysis and CAPA Investigations for the Life Sciences
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Upcoming Events
24
May
Powering an Effective Oversight Strategy with Clinical and Operational Insights
25
May
2022 WCG Avoca Quality & Innovation Summit: Own the Future
21
Jun
Medical Device Reporting: Best Practices and Common Pitfalls
22
Jun
Meet CDRH’s New Strategic Priorities: Where the Center is Headed and How Devicemakers Can Keep Up
28
Jun
Effective Root Cause Analysis and CAPA Investigations for the Life Sciences
Featured Products
Biological Risk Evaluation and Management for Medical Devices
GMP Inspection Preparation Checklist: A Tool for Internal Auditing
Featured Stories
Linear Health Sciences Gets FDA Clearance for Its Orchid Safety Release Valve
Roche’s Faricimab Gains UK Approval Via International Program
Becton Dickinson Gets FDA Clearance for Its Molecular Diagnostic Platform
Bayer Backs Out of $670 Million Collaboration Deal With Atara
The Revised ICH E8:
A Guide to New Clinical Trial Requirements
Learn More
