Clinical Investigation FAQ
What are clinical investigations according to the EU MDR?
Why is clinical data required? What types of clinical investigation can be conducted?
We have all the answers and more…
What are clinical investigations according to the EU MDR?
Why is clinical data required? What types of clinical investigation can be conducted?
We have all the answers and more…
What is a Clinical Development Plan (CDP) under the EU MDR?
Why is it important? How does it differ?
We answer these questions and more…
Clin-r+ outlines the requirements and considerations manufacturers should review to ensure that Clinical Investigations they undertake are well researched to ensure a return on investment.
Clinical Investigations for Medical Devices and IVD Read More »
The Clinical Development Plan (CDP) is a new document that you must complete for the EU MDR Technical Documentation. Clin-r+ explains how it’s an important strategic document that can help MedTech align development and regulatory requirements.