ISO 20417 – all you need to know
When a manufacturer provides a medical device to the market, the manufacturer has to supply information with the device. As this is defined in EN… Read More »ISO 20417 – all you need to know
When a manufacturer provides a medical device to the market, the manufacturer has to supply information with the device. As this is defined in EN… Read More »ISO 20417 – all you need to know
Being involved in countless projects and client interactions regarding questions to GACP, the following 5 most prominent myths are explained. Myth 1 – I can… Read More »5 Myths about GACP
understanding the classification rules The Medical Device Regulation (MDR) EU 2017/745 defines in its Annex VIII the classification rules for medical devices. Read here how… Read More »Classification Rules under the MDR