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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

Evan Phelps -Teal

Breakthrough Medical Devices – Webinar Recording/Transcript

$287.00
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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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