CRFWEB‘s core attributes makes it the perfect option for post-approval or post-market research. Our super-fast, DIY set-up option and simplicity of use, makes it ideal for putting together studies where turnaround time is of the essence and flexibility is paramount.
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Post-Market, Post-Approval Studies
Post-Marketing for Medical Devices
While CRFWEB is suitable for any post market studies, the MDR and IVDR regulations in Europe have upped the significance for medical devices in particular. If you want to market your medical device in Europe, you will need to meet compliance requirements, whether your appliance is new to market or already there. You will also need to provide ongoing evidence with respect to safety and efficacy.
With the ability to deliver subject-led data capture via the CRFWEB App, our ePRO and eDIARY modules are of particular benefit to those looking at post market evaluation.
Contact us today to arrange a web demo and see how we can assist your post market evaluations.
