A Guide to App Compliance & Regulation

This article looks at some of the reasons we should be considering compliance as part of medical app development, the barriers faced and thoughts on how to achieve and happy medium between developers and regulatory authorities.

Here’s a sample of what you can expect to find in the white paper and what else it contains.

Introduction

The MHRA recently released new guidance notes on medical device stand-alone software (including apps) and it helps to clarify which types of apps should be classified as medical devices. It still requires developers to understand the implications of the EU Medical Device Directive but helps to identify through the use of words and phrases which apps could be classed as medical devices. This article looks at some of the reasons we should be considering compliance as part of medical app development, the barriers faced and thoughts on how to achieve a happy medium between developers and regulatory authorities.

To request a copy please email: sales@geneticdigital.co.uk

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