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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
Jun. 13, 2023
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Jun. 13, 2023
Winners Only: 3 Steps to Compete in Digital Quality
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Webinar
Jun. 20, 2023
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Jun. 20, 2023
What’s CSA? And how can it streamline your GxP System Verification?
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Webinar
Jun. 22, 2023
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Jun. 22, 2023
Transforming Life Sciences Training: Top Trends Shaping Enterprise Learning Strategies
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Webinar
Jul. 12, 2023
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Jul. 12, 2023
FDA’s New Sterilization Pilot on Risk-Based Cleaning and Disinfectant Programs: Best Practices for Quality, Regulatory and Compliance Professionals
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Upcoming Events
06
Jun
Gene & Cell Therapy Regulation: Comparability and Other New Developments
07
Jun
Developing World-Class SOPs: Optimizing Quality and Compliance
08
Jun
Implementing ICH E8 R1 Recommendations Increases Site and Participant Relationship Scoring Measures
13
Jun
Winners Only: 3 Steps to Compete in Digital Quality
14
Jun
Pharmaceutical Quality Risk Management and ICH Q9(R1): Navigating the Global Intersection of Principle and Regulation
20
Jun
What’s CSA? And how can it streamline your GxP System Verification?
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FDA’s New Quality System Regulation: Transitioning from QSR to ISO 13485
Selecting and Implementing Electronic Document Management Systems in the EU
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The Revised ICH E8:
A Guide to New Clinical Trial Requirements
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