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What we learnt from taking a mobile app through MHRA compliance

Read about how we launched an app that conforms to the EU Medical Device Directive for a client who are now registered as a Class 1 device manufacturer.

Mobile app medical compliance

We launched an app that conforms to the EU Medical Device Directive 2007/47 EC for Rosemont Pharmaceuticals who are now registered as a Class 1 device manufacturer. The MHRA have recently released guidance on what constitutes a medical device for apps but this guidance was unavailable when we took this client through the process and this is what we learned.The Rosemont Pharmaceuticals App acts as both a product reference guide and as a liquid medicine dosage calculator for use by healthcare professionals.
Read the full story on our bog: http://www.geneticapps.co.uk/2014/04/taking-an-app-through-compliance/

29th April 2014

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