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Drugs and Medical Devices Seminar, Denver, CO

5.11.14 | Filed Under: News

 

General Information:

  • “Promoting Public Health, Fostering Uniformity, and Establishing Partnerships”
  • Association of Food and Drug Officials (AFDO) Drugs & Medical Devices Seminar
  • Co-Hosted by the Western Association of Food and Drug Officials
  • Co-sponsored by the U.S. Food and Drug Administration & Rocky Mountain Regulatory Affairs Society
  • Dates: June 23-24, 2014
  • Location: Grand Hyatt Denver, Denver, Colorado

FDA and Global Engagement:

  • Progress on the Pathway to Global Product Safety.
  • This seminar will primarily be attended by industry representatives from the pharmaceutical and medical device community as well as federal and state regulatory officials.
  • Topics for discussion include the following:
    • Medical Device Single Audit Program,
    • Contract Manufacturing Arrangements for Drugs,
    • Compliance Question Panel featuring Key FDA Representatives,
    • Medical Device Recalls,
    • Compounding Pharmacies,
    • Comparison of EU and US Device GMP Requirements,
    • UDI Implementation,
    • Pharmaceutical Inspection Co-operation Scheme,
    • and Biosimilars Regulations.
  • For more information visit: http://denver.afdo.org/
  • Federal Register Notice: https://www.federalregister.gov/articles/2014/03/31/2014-07059/the-food-and-drug-administration-and-global-engagement-progress-on-the-pathway-to-global-product
  • AFDO is an international non-profit organization devoted to developing strategies to resolve and promote public health and consumer protection issues related to the regulation of foods, drugs, medical devices, and consumer products. Membership includes individuals from local, state and federal regulatory agencies, regulated industry, and academia who are concerned with the development and enforcement of uniform food, drug, and consumer product safety laws and regulations.

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