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fda-emergency-use-authorization-guidance
Press Release
May 12, 2020
MethodSense Releases LuminLogic Version 7.0 in Support of Medical Device Companies' Compliance Efforts
LuminLogic 7.0 enables Medical Device Companies to expand their regulatory compliance efforts in a virtual compliant environment.
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Press Release
May 6, 2020
MethodSense CEO Selected as Panelist for Larger Than Life Science Event
Rita King will sit on discussion panel about the future impact of COVID-19 on medical technologies and the delivery of medicine.
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Press Release
Apr 29, 2020
MethodSense Creates Resource Website to Assist in Medical Device FDA Authorization Submissions
Morrisville, N.C., company provides resources and direction for medical device authorization under FDA Emergency Use Authorization Guidance.
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