We are delighted to launch an updated Medical Device Consultancy and Training offering. We have experienced an unprecedented period of change within the medical device and in vitro diagnostic sector over the last five or six years, but things will continue to be in a state of flux for the next few years. We have the changing timelines for the full implementation of EU MDR, we have the introduction of the UK’s new legislation and seemingly endless ‘transition periods’.
Even with annual Notified/Approved body inspections, keeping on top of everything can be difficult and with the ever-increasing costs of Notified/Approved body involvement getting non-conformances can have a serious financial impact. With so many changes it is vital to plan ahead and to make sure you are only doing things once and if possible combining as many as possible. We can provide an independent assessment of your current position and readiness for upcoming changes, producing a detailed GAP analysis. We can provide tailored training for your particular situation or sector, to make the most efficient use of your valuable resources.
For more information on Medical Devices please visit our dedicated page.
To book one of our courses please visit our bookings page or to book a meeting with one of our consultancy team visit our enquiry page.
