MedTech Compliance Articles
Expert guides on EU MDR, Clinical Evaluation, and Literature Review strategies.
CiteMed | EU MDR & Clinical Evaluation Insights
In-depth articles and resources on EU MDR, IVDR, and clinical evaluation for regulatory affairs professionals.
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Medical Device Development: When Should you do Clinical Evaluation?
The medical device development process is not a one-step [...]
Your Medical Device Got CE Marked – Now What?
Obtaining the CE mark is one of the most [...]
Navigating Medical Device Safety, Regulation, and Adverse Europe
Adverse Events in Europe The landscape of medical device [...]
Literature Search Protocol for EU MDR: When and How to Update Your Review
Getting the long-awaited CE mark is certainly something to [...]
Switzerland’s Medical Device Regulation and the EU Regulations
The medical device industry is thriving globally. Not only [...]
Updates To The EU Blue Guide: Impacts on Market Surveillance of Medical Devices
In July 2021, Regulation (EU) 2019/1020 on market surveillance [...]