by IMed Consultancy | May 2, 2023 | IVD, PMS, UKRP
Planning and Process for Compliant Post-Market Surveillance STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe Deadlines for Medical Devices Regulation (EU) 2017/745 (MDR) and the In Vitro...
by Matt Burton | Mar 22, 2023 | IMed Consultancy, IVD, MDR, New Markets, PMS, UKRP
UKCA opportunity – A compelling case for UK market access and commercial opportunity STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe The medical device regulatory environment is undergoing...
by Matt Burton | Feb 21, 2023 | IMed Consultancy, MDR, UKRP
Countdown to the final UK MDR: changes Importers and Distributors need to be aware of STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe The final UK Regulation text is due to be published from...
by Matt Burton | Feb 8, 2023 | IMed Consultancy, MDR, UKRP
STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe The final UK Regulation text is scheduled to be published from Spring 2023, so manufacturers should be assessing their current provider to...
by Jonathan Ripley | Dec 1, 2022 | Clinical Writing, IMed Consultancy, IVD, MDR, Medtech Marketing, PMS, swiss, UKRP
Switzerland’s Parliament Moves to Accept FDA approved Medical Devices STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe On the 28 Nov 2022, Switzerland’s Parliament took a decision to...
by Matt Burton | Dec 1, 2022 | Academy, Clinical Writing, IMed Consultancy, IVD, MDR, Medtech Marketing, PMS, UKRP
How to advertise your medical devices in the UK and avoid enforcement. STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe The control of advertising medical devices in the UK is based on a...
by Matt Burton | Dec 1, 2022 | IMed Consultancy, IVD, MDR, Medtech Marketing, UKRP
Have you appointed the right UKRP? Part 3 STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe This is the 3rd article in a 3 day, 3-part series which considers some of the upcoming changes to the...
by Matt Burton | Dec 1, 2022 | Academy, Clinical Writing, IMed Consultancy, MDR, Medtech Marketing, UKRP
Have you appointed the right UKRP? Part 2 STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe If you are currently providing a UKRP service or if you are an Ex-UK Medical Device or IVD...
by Matt Burton | Nov 30, 2022 | Academy, Clinical Writing, IMed Consultancy, IVD, MDR, Medtech Marketing, PMS, UKRP
Have you appointed the right UKRP? – Part 1 STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe If you are currently providing a UKRP service or if you are an Ex-UK Medical Device or IVD...
by Jonathan Ripley | Nov 30, 2022 | Clinical Writing, IMed Consultancy, IVD, MDR, Medtech Marketing, PMS, UKRP
The Regulatory Framework in Switzerland – Ordinances and CH-REPs STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe Switzerland, though not a member state of the European Union, worked under a...
