dicentra
dicentra is a Toronto-based regulatory consulting firm and CRO serving medical device and other health-product companies. Its device team provides FDA and Health Canada regulatory strategy, agency liaison, submission support, clinical trial planning and post-market reporting. For diagnostics, wearables and software-driven devices, dicentra also supports 510(k), De Novo, PMA and Q-Submission evidence planning and regulator engagement.
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DNV Product Assurance
updated about 2 years ago
Registering a UDI with GS1 (Unique Device Identifiers for Medical Devices)
Dr. Oliver Eidel
31 views
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8 months ago
MDCG guidance
MDCG 2025-4: Medical device software apps on online platforms
How MDR/IVDR and Digital Services Act responsibilities apply when medical device software apps are offered through app stores and online platforms.
Software
Endorsed Jun 2025