Transparency advocates win victory for public access to clinical trial data | Center for Science in the Public Interest
Leveraging Real World Evidence in Regulatory Submissions of Medical Devices | FDA
U.S. Food and Drug Administration
New data adds to X4's hopes on FDA approval in WHIM
FDA Approval for Resascope Soft - AMS Group
Lumma is FDA registered. I saw they updated their website i week ago stating they were, and i went to the FDA site and they are. Link: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm : r/menstrualcups
Label (PDF) - Accessdata FDA - Food and Drug Administration
FDA begins data initiative with millions of adverse event reports - PMLiVE
Label (PDF) - Accessdata FDA - Food and Drug Administration
FDA Data Integrity Enforcement Trends and Practical Mitigation Measures - Food and Drug Law Institute (FDLI)
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PDF) How to access and process FDA drug approval packages for use in research
July 6, 2022 (https://www.accessdata.fda.gov/scripts/foi/FOIRequest/requestinfo.cfm) Food and Drug Administration Division of Fr
FDA Expands EHR Data Analytics with Active Surveillance System
GAO-17-564, Accessible Version, INVESTIGATIONAL NEW DRUGS: FDA Has Taken Steps to Improve the Expanded Access Program but Should
Drugs | FDA
accessdata.fda.gov Cross Site Scripting vulnerability OBB-134618 | Open Bug Bounty
U.S. FDA on Twitter: "FDA launches interactive database with crucial information about life-saving, HIV drugs available for purchase under the PEPFAR program as part of ongoing mission to empower the public through
FDA Explains How to Craft a Data Management Plan | RAPS
Expanded Access (Compassionate Use) Submission Data | FDA
Investigational New Drugs: FDA Has Taken Steps to Improve the Expanded Access Program but Should Further Clarify How Adverse Events Data Are Used | U.S. GAO
FDA-ARGOS is a database with public quality-controlled reference genomes for diagnostic use and regulatory science | Nature Communications
FDA: Medical Device Orgs Must Offer Patient Access to Health Data
