Collection: Fast Track Requests
FDA documents available for fast-track requests typically delivered within 1 to 2 weeks. Our fast-track request service identifies previously requested and redacted documents for quick access.
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FDA FAERS Mydriasis Case Narratives – Isoflurane
Regular price $69.00 USDRegular priceUnit price / per -
FDA Review Documents – Diastat AcuDial (NDA: 020648)
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FDA FSVP Import Entries – Thrive Market, Inc.
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FDA EIR – Patheon Pharmaceuticals Inc., Cincinnati, OH (FEI 1510437), ID 1204466
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FDA FAERS Adverse Event Narratives – Semaglutide and Tirzepatide (Feb–Oct 2024)
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FDA FSVP Import Data Request – Lipari Foods, Swiss American (Oct 2022–Oct 2024)
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FDA FSVP Import Data Request – Dollar Tree, Greenbrier International (Oct 2022–Oct 2024)
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FDA 483 Reports for Japanese Companies – Daiichi Sankyo, Takeda, Others
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FDA FAERS Reports – Nicotine Product Case Summaries
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FDA Pharmacology/Toxicology Review – Timoptic NDA018086
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FDA FAERS Case Report – Betamethasone Dipropionate/Calcipotriene (Case ID: 24310038)
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FDA FSVP Data Request – TJX Brands (Oct 2022–Oct 2024)
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FDA 483 Reports – Safecor Health, LLC (FEIs: 1218914, 3008841077)
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FDA Individual Case Reports – Multiple FAERS IDs
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FDA FAERS Reports – SYFOVRE (APLS)
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FDA FAERS Reports – IZERVAY
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FDA FAERS Reports – Daybue (ACAD)
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FDA FAERS Reports – Rezdiffra
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FDA FAERS Reports – Zurzuvae
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FDA FAERS Reports – Rytelo (GERN)
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FDA FSVP Importer Records – 2024
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FDA Adverse Event Reports – Multiple Case IDs
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FDA 483 and EIR – Fujifilm Diosynth Biotechnologies UK Ltd. (FEI 3007182567), Mar 2023
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FDA FAERS Report – SYFOVRE (Pegcetacoplan) Oct 2024
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FDA FAERS Case Report – 24283702
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FDA 483 Inspection Reports – Patheon France S.A.S. (FEI 3004468553), Jun–Nov 2024
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FDA 483 Reports – Unit Dose Services, LLC (FEI 3010164341)
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FDA Approved Label Info – ANDA #212138, #212198
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FDA Form 483 – Pedro A. Velasquez-Mieyer, M.D. (FEI 3031753125), Sep 2024
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FDA Entry-Line Records – United Safety Agents (Oct 2024)
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FDA List of Email Addresses
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FDA Drug Information Request – Zyloprim
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FDA Adverse Event Reports and SBA – OXBRYTA (Voxelotor)
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FDA Adverse Event Narratives – Semaglutide (Pre-July 22, 2024)
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FDA Documents Relating to FCN 1352
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FDA List of CBER Approvals for 1997
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