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The Composition and Value of a Portfolio Analysis

Camargo

DECEMBER 22, 2021

For example, streamlined programs can be limited to literature searches, nonclinical studies, demonstration of bioequivalence to an approved product, or a combination of nonclinical and bioequivalence studies, and their relatively low costs may be appealing. Clinical Pharmacology. This is a key factor in designing Phase 2 and 3 trials.

Bioequivalency 169
Bioequivalency Production Genotoxicity In-Vivo 169
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In the News: October Regulatory and Development Updates

Camargo

NOVEMBER 11, 2020

Each month, Camargo’s “In the News” series highlights important changes and advancements in the regulatory and development space and explores how those changes could impact your program. Unpacking the (Black) Box: Antares Licenses Urology Product with Boxed Warning. of hyponatremia, or low blood sodium levels. In October, the U.S.

Development 242
Development Bioequivalency Generic Drugs Production 242
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