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Veterans Affairs, Veterans Health Administration
Wilmington, Delaware, Delaware
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Veterans Affairs, Veterans Health Administration
Singapore, Singapore,
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Veterans Affairs, Veterans Health Administration
Ann Arbor, Michigan, Michigan
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Veterans Affairs, Veterans Health Administration
Battle Creek, Michigan, Michigan
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Duke University Health System
Warsaw, North Carolina
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Veterans Affairs, Veterans Health Administration
Hampton, Virginia, Virginia
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Veterans Affairs, Veterans Health Administration
Martinsburg, West Virginia, West Virginia
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Veterans Affairs, Veterans Health Administration
Temple, Texas, Texas
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Veterans Affairs, Veterans Health Administration
Cleveland, Ohio, Ohio
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Veterans Affairs, Veterans Health Administration
Wilmington, Delaware, Delaware
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Veterans Affairs, Veterans Health Administration
Charlotte, North Carolina, North Carolina
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Veterans Affairs, Veterans Health Administration
Atlanta, Georgia, Georgia
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Veterans Affairs, Veterans Health Administration
Wilmington, Delaware, Delaware
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AD Regulatory Affairs
500 million patients were touched by Sandoz generic and biosimilar medicines in 2020 and while we're proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world. Directs the development of submission of product registration, progress reports,supplements, amendments, and/or periodic experience reports. Provides strategic product direction to teams on interaction and negotiates evidence with regulatory agencies.Interacts and negotiates with regulatory agency personnel in order to expedite approval of pending registration and answers any questions. Serves as a regulatory liaison on the project team throughout the product lifecycle. Ensures rapid and timely approval on of new drugs, biologics/biotechnology and/o
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