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Featured Product In Books

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

Dan O’Leary purple the one

BREXIT’s Impact on Medical Devices – Webinar Recording/Transcript

$287.00
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Alan G. Minsk, Esq. - green

Drug, Biologics and Combination Products Labeling – Webinar Recording/Transcript

$287.00
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Grace Fu Palma-Jason Liang-Dan Goldstein-red

Latest Medical Device Postmarket Surveillance Requirements from China’s NMPA and the U.S. FDA – Webinar Recording/Transcript

$287.00
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Data Integrity for Drug and Device Manufacturers

Data Integrity for Drug and Device Manufacturers: Avoiding Breaches and Closing Gaps

$397.00
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Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

Spreadsheet Validation: Tools and Techniques to Make Data in Excel Compliant

$397.00
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Sue Schniepp Virtual Conference - blue

Data Integrity in the COVID-19 Era and Beyond — Part III: The Real-World Costs of Data Integrity – Virtual Conference Recording/Transcript

$287.00
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Chris-Markus-Jessica-Ringel-Quynh-Hoang-blue

Get Your Combination Products to Market Faster – Webinar Recording/Transcript

$287.00
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Joanna Brougher - green

Patents & FDA Regulation of Pharmaceutical Products – Webinar Recording/Transcript

$287.00
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New Adverse Event Reporting Procedures

New Adverse Event Reporting Procedures: A Devicemaker’s Guide to the IMDRF Code Transition

$397.00
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GMP Inspection in the EU

GMP Inspection in the EU: Avoiding 12 Common Pitfalls

$397.00
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Karla Palmer teal

Pharmacy Compounding Regulation – Webinar Recording/Transcript

$287.00
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Keith Webber, Ph.D- purple

FDA’s Guidance on Drugs and Biologics During COVID-19 – Webinar Recording/Transcript

$287.00
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