[FEATURED] Calls For More Patient Input In Medical Device Development and Regulation
It is vital to involve patients in medical device development, regulatory assessments, and post-marketing activities. The European Patients’ Academy on Therapeutic Innovation (EUPATI) has explained why and what it is […]
Medtech Insight’s Guidance Tracker
Author: Criterion Edge Writers Staying current with national and international regulatory updates is a constant challenge for those in the medical device industry. Medtech Insight, already known for their website […]
[FEATURED] Regulators Urged To Avoid ‘Conflicting’ Clinical Requirements For Drug-Device Combinations In EU
EU regulators are being urged to get their skates on and publish guidance on new clinical requirements that will kick in soon for integral drug-device combination products.
