Understanding FDA Inspections and Data

Поділитися
Вставка
  • Опубліковано 18 вер 2023
  • FDA provides an overview of drug manufacturing inspections; a general understanding of Current Good Manufacturing Practices (CGMPs) and FDA Inspections; and demonstrates where inspection data is found on FDA’s website and share how to navigate the FDA Inspection Dashboard.
    Timestamps
    01:35 - Applicable Manufacturing Standards
    10:22 - Understanding CGMP Inspections and 483s
    24:39 - FDA Regulatory Actions & How FDA Reviews Inspectional Findings
    39:21 - Where to Find Inspection & Other Compliance Documents
    41:45 - FDA Inspections Dashboard Demo
    49:04 - Q&A Discussion Panel
    Speakers | Panelists:
    Jennifer Maguire
    Director, Office of Quality Surveillance (OQS)
    Office of Pharmaceutical Quality (OPQ)
    Center for Drug Evaluation and Research (CDER)
    FDA
    Simone Pitts
    Pharmaceutical National Expert
    Office of Regulatory Affairs (ORA) | FDA
    Francis Godwin
    Director, Office of Manufacturing Quality (OMQ)
    Office of Compliance (OC) | CDER | FDA
    Darshini Satchi
    Deputy Director, Division of Information Disclosure Policy (DIDP)
    Office of Regulatory Programs (ORP) | CDER | FDA
    Rob Bughman
    Project Manager, FDA Inspection Dashboard
    ORA | FDA
    Learn more at: www.fda.gov/dr...
    -----------------------
    FDA CDER’s Small Business and Industry Assistance (SBIA) educates and provides assistance in understanding the regulatory aspects of human drug products & clinical research.
    Upcoming Training - www.fda.gov/cd...
    SBIA Listserv - public.govdeli...
    SBIA 2022 Playlist - • 2022 CDER Small Busine...
    SBIA LinkedIn -  / cder-small-business-an...
    SBIA Training Resources - www.fda.gov/cd...
    Twitter -  / fda_drug_info
    Email - CDERSBIA@fda.hhs.gov
    Phone - (301) 796-6707 I (866) 405-5367

КОМЕНТАРІ •