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Celldex Therapeutics, Inc

New Haven, Connecticut

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Allurion Technologies

01760, Massachusetts

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Overjet

Boston, Massachusetts

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Eupraxia Pharmaceuticals

Canada

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Beckman Coulter, Inc.

Chaska, Minnesota

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Asensus Surgical

Durham, North Carolina

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Asensus Surgical

Durham, North Carolina

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Asensus Surgical

Durham, North Carolina

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EPM Scientific

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EPM Scientific

Waltham, Massachusetts

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EPM Scientific

Cambridge, Massachusetts

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Kindred Healthcare

St. Petersburg, Florida

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National Quality Forum

Washington, D.C.

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Washington, D.C.

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Plainsboro, New Jersey

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MemorialCare Health System

Laguna Hills, California

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AdventHealth

Hendersonville, North Carolina

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Kindred Healthcare

Ocala, Florida

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Share Our Selves Community Health Center

Newport Beach, California

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Kindred Healthcare

Chandler, Arizona

Sarasota Memorial Hospital - Sarasota, FL

Sarasota, Florida

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Manager, Regulatory Affairs
What Regulatory Affairs (NPHS Drug Manufacturing) contributes to Cardinal Health  Regulatory Affairs (NPHS Drug Manufacturing) is responsible for regulatory filings (such as abbreviated/new drug applications, drug master files, supplements, establishment registrations, and PDUFA/GDUFA fee payments) and compliance with regulatory agency requirements (such as annual reports, labeling requirements, regulatory aspects of change management, and participation in inspections if/as needed) regarding drug products, APIs, intermediates, and starting materials. In short, drug lifecycle management for an active portfolio of drugs, as well as filing applications for new drugs.   


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