Gemini Workshop @ FDA White Oak - 10-11 December - REGISTER SOON!
Bell, Sarah
The HL7-IHE Gemini Device Interoperability community has just completed two weeks of meetings in Germany, starting with the 4th SDPi Developers & Testers Workshop, and followed by a Regulatory (EU NB) + Conformity Assessment workshop, both very productive, setting the stage for a strong entry into 2025!
The final workshop for 2024 is coming next:
This HYBRID event at the FDA White Oak Campus in Silver Spring, MD (Washington D.C. area) is a follow on to the EU NB workshop, but has a focus on the U.S. FDA program aspects.
Again, the first day has a Regulatory Pathway focus and the 2nd day a Conformity Assessment program focus.
ROOM IS LIMITED AT THE FDA + INTERNATIONAL PARTICIPANTS WILL REQUIRE ADDITIONAL TIME AND PAPERWORK!!
Let us know by 26 November if you intend to participate in person and are not a U.S. citizen.
We will be updating details to the agenda linked above, especially based on the results of the recent regulatory workshop in Stuttgart, including additional presenters and topic detail.
REGISTRATION is open and free with details on the linked Confluence page above. (simply send an email to myself and Isabel Tejero (Isabel...@fda.hhs.gov)
Please let me know if you have any questions. PLEASE FORWARD THIS EMAIL to anyone you think would be particularly interested in the workshop topics.
Thank you,
~ > Todd
IHE SDPi Profiles for PRACtical Interoperability
IM: ToddCooperAFC
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