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FDA MedWatch Reports for 9 Cases from Multiple Countries Including Mylan, Aurobindo, Takeda, Incyte, Astellas
FDA MedWatch Reports for 9 Cases from Multiple Countries Including Mylan, Aurobindo, Takeda, Incyte, Astellas
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Original Request: MedWatch Reports for the following 9 cases: IT-MYLANLABS-2024M1091762 IT-AUROBINDO-AUR-APL-2024-049628 IT-TAKEDA-2024TUS100811 NVSC2024IT196107 GB-INCYTE CORPORATION-2024IN009439 US-INCYTE CORPORATION-2022IN006886 US-ASTELLAS-2017US016366 PL-INCYTE CORPORATION-2019IN002214 PHHY2017IT166445
Tags: Pharma, Adverse Event, 2024
Tags: Pharma, Adverse Event, 2024
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. IMPORTANT: The FDA FOIA office operations are currently suspended. We are happy to make the request but do not know when we will receive a response. Learn more about Fast-Track Requests here.
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