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Guidance Documents/Guidance-Document/Assessing User Fees Under the Biosimilar User Fee Amendments of 2022: Guidance for Industry

Assessing User Fees Under the Biosimilar User Fee Amendments of 2022: Guidance for Industry

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

July 31, 2023

July 27, 2023

Center for Drug Evaluation and Research

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