Cyber security is vital for patient safety, for data security and for data integrity; it’s important that you understand the drivers, regulation and what you can do to ensure your devices are safe and secure.
DetailsThe regulatory landscape for medical devices is presently very challenging. Industry is well aware that the 3 year transition period from a directive to a regulation ends on the 15th of May 2020, whereupon the new regulatory framework (MDR) will apply in full. This will be followed in May 2022 with the new IVD regulations.…
Medilink UK, Greater Birmingham Chambers of Commerce and the Economic Development Board Mauritius recently came together to discuss potential mutual benefits for the UK and Mauritius economy through medical device manufacturing. Mauritius has built a well-developed medical devices industry that produces a wide range of highly sophisticated products and this sector is expected to play a…
Free to attend half day workshop, providing best practice tools and tips to ensure your product and organisation is cyber safe.
DetailsThe Medicines and Healthcare products Regulatory Agency (MHRA) have provided details of legislation to ensure continuity of supply of medicines, medical devices and clinical trials in a no deal Brexit. Leaving the EU with a deal remains the Government’s top priority. This has not changed. However, a responsible government must plan for every eventuality, including…
Medical devices and clinical consumables supply in a March 2019 no-deal scenario: an update The Secretary of State for Health and Social Care has written to health and care providers to update them on medical device preparations for a potential no-deal Brexit. The Secretary of State for Health and Social Care, Matt Hancock, has written…