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Accelerating-Generic-Drug-Development

Accelerating Generic Drug Development: The FDA’s New Plan for Increasing Generic Competition

$397.00
Accelerating Generic Drug Development explains the FDA’s new policy and shows how to navigate the new pathway to approval. Read More

Books

Jay Crowley red

Meeting Global Unique Device Identification Requirements – Webinar Recording/Transcript

$287.00
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Amanda McFarland - blue

Pharmaceutical Quality Risk Management – Webinar Recording/Transcript

$287.00
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Sue Schniepp Virtual Conference - blue

Data Integrity in the COVID-19 Era and Beyond — Part I: The Impact of COVID-19 – Virtual Conference Recording/Transcript

$287.00
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Sarah Lyons and Vivien Fagan - purple

Pharmaceutical Clinical Trials Transparency and Privacy – Webinar Recording/Transcript

$287.00
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Dan O’Leary teal

Inspection, Measuring and Test Equipment – Webinar Recording/Transcript

$287.00
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Scott R. Burger - green

Overcoming Comparability Issues in Regenerative Medicines Manufacturing – Webinar Recording/ Transcript

$287.00
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Jon Gimbel

EU-MDR Postmarket Surveillance – Webinar Recording/Transcript

$287.00
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Steve Walfish- teal

How to Address Medical Device Sample Size Issues – Webinar Recording/Transcript

$287.00
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Postmarket Surveillance Under EU-MDR

Postmarket Surveillance Under EU-MDR: Preparing for New Requirements

$397.00
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Usability Engineering: How the Updated ISO 14971:2019 Changes Your Process

Medical Device Safety in the Magnetic Resonance Environment – Webinar Recording/Transcript

$287.00
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06-24-20-Are-You-Ready-for-ISO-149712019-Recording.png

Are You Ready for ISO 14971:2019? – Webinar Recording/Transcript

$287.00
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Devicemaker’s Guide to Quality System Change Management

Devicemaker’s Guide to Quality System Change Management

$397.00
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