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  1. How should #FDA inform the public about inspection results? Submit your idea on FDA blog http://bit.ly/6k0gYQ #medicaldevice
  2. Deadline for device establishment annual registration 12/31/09 http://bit.ly/10u2rv #medicaldevice
  3. File radiation safety (product) reports for radiation-emitting products online with #FDA eSubmitter http://bit.ly/6EbSkO
  4. Medical Device Reporting (MDR)-Contact information for user facilities & manufacturers http://bit.ly/8865p8 #fda #medicaldevice
  5. Reminder: Ear, Nose & Throat Devices Panel Mtg 12/18 http://bit.ly/7ecC4z
  6. Reminder: Gastroenterology & Urology Devices Panel Mtg 12/11 http://bit.ly/6fBa7E
  7. FDAcdrhIndustry doesn't respond 2 replies or direct messages on Twitter. Please direct all questions & comments 2 dsmica@fda.hhs.gov
  8. Complaint, ? or dispute - scientific, regulatory, or procedural nature? Contact CDRH ombudsman http://bit.ly/7AF0XX #medicaldevice #fda
  9. Registration & Listing: #FDA does not use outside contractors 2 notify or bill regulated industry http://bit.ly/10u2rv #medicaldevice
  10. Have a question about a medical device or radiation-emitting product? Call or e-mail http://bit.ly/6SRAq1 #fda #medicaldevice
  11. Endoscopes - Safety Communication: How 2 prevent cross-contamination when cleaning & sterilizing http://bit.ly/10UO3f #fda #medicaldevice
  12. Medical Device Reporting-Electronic Submission Requirements: Last day to submit comments http://bit.ly/y6hSv #fda #medicaldevice
  13. Want to get your radiation-emitting product on the market? Here's what you need to know http://bit.ly/4zljqg #fda #medicaldevice
  14. General & Plastic Surgery Devices Panel to meet 03/25/10 http://bit.ly/2oMWC7 #fda #medicaldevice
  15. National Mammography Quality Assurance Advisory Committe to meet 01/25/10 http://bit.ly/1xPDf8 #fda #medicaldevice
  16. Premarket Approvals (PMAs) for Oct '09 http://bit.ly/XaJ7F #fda #medicaldevice
  17. Need to update your firm's registration & listing info? Check here http://bit.ly/4lvru2 #fda #medicaldevice
  18. In Vitro device manufacturers: Electronically complete and submit 510(k) applications http://bit.ly/39NvPR #FDA #medicaldevice
  19. R u required to pay establishment registration user fees? Here's how payment process works http://bit.ly/15jfQp #fda #medicaldevice
  20. RT @FDAWomen Listen live: FDA Public Hearing on Internet and #socialmedia tools: http://bit.ly/2yotDt