All Posts by crfadmin

Beat the clock to medical device compliance

Beat the clock to medical device compliance

MDR and IVDR regulations in Europe and similar moves to tightening compliance across the globe have led to a lot of concern in the medical device industry. New devices need to demonstrate compliance, existing devices need to show compliance and all devices need to demonstrate compliance on an ongoing basis.

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Post-Approval-and-Post-Marketing-Research

The end of the paper trial?

It’s time to move on from paper. No Really. It is time to move on from paper. Since the launch of CRFweb, the Clindox team have been banging the drum about the end of paper -based clinical trials. As suppliers of an EDC application with eCRF, ePRO , eTMF you could argue

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MEDICAL-CODING

Reaping the Benefits of Medical Coding

Adopting standardised medical terminology has clear benefits to all parties in the clinical trial process. Firstly it reduces the risk of confusion and misunderstanding of terminology used among the different parties involved in the trial. If used from the outset, it also reduces the need to translate/convert data from one

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