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Research and Development
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
Jul. 14, 2020
EU-MDR Postmarket Surveillance: Best Practices for Medical Device Regulatory, Compliance & Quality Specialists
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Webinar
Jul. 15, 2020
How to Address Medical Device Sample Size Issues: What Regulatory and Quality Professionals Absolutely Must Know
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Webinar
Jul. 16, 2020
Micro-learning, Macro-Compliance: Improving GxP Compliance with Modern Learning Techniques
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Webinar
Jul. 16, 2020
Inspection, Measuring and Test Equipment: A Regulatory Approach
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Webinar
Jul. 29, 2020
Meeting Global Unique Device Identification Requirements: Regulation, Compliance and Best Practices
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Virtual Conference
Aug. 04, 2020
Data Integrity in the COVID-19 Era and Beyond — Part I: The Impact of COVID-19: Complying with Data Integrity Guidelines in the Midst of a Pandemic
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Webinar
Aug. 06, 2020
Upgrade Your Medical Device Recall Strategy: Regulatory and Business Considerations
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Upcoming Events
14
Jul
EU-MDR Postmarket Surveillance: Best Practices for Medical Device Regulatory, Compliance & Quality Specialists
15
Jul
Predictive Compliance Risk and Quality Management: A New Digital Paradigm for the Post-COVID-19 World
15
Jul
How to Address Medical Device Sample Size Issues: What Regulatory and Quality Professionals Absolutely Must Know
16
Jul
Micro-learning, Macro-Compliance: Improving GxP Compliance with Modern Learning Techniques
16
Jul
Inspection, Measuring and Test Equipment: A Regulatory Approach
22
Jul
Overcoming Comparability Issues in Regenerative Medicines Manufacturing: The Latest on Cell and Gene Therapy Regulation
Featured Products
Biological Risk Evaluation and Management for Medical Devices
GMP Inspection Preparation Checklist: A Tool for Internal Auditing
Featured Stories
New Data Shows Gilead’s Remdesivir Improves Recovery for COVID-19 Patients
FDA to Resume Domestic Inspections Using New Assessment System
Pfizer and BioNTech Nab Fast Track Status for Two COVID-19 Vaccines
Vela’s Automated COVID-19 Test Gains CE Mark
The Revised ICH E8:
A Guide to New Clinical Trial Requirements
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