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Planning and Process for Compliant Post-Market Surveillance

Planning and Process for Compliant Post-Market Surveillance

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...
UKCA opportunity – A compelling case for UK market access and commercial opportunity

UKCA opportunity – A compelling case for UK market access and commercial opportunity

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...
Countdown to the final UK MDR: changes Importers and Distributors need to be aware of

Countdown to the final UK MDR: changes Importers and Distributors need to be aware of

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...
The new UK Medical Device Regulation is due soon: is your appointed UKRP ready?

The new UK Medical Device Regulation is due soon: is your appointed UKRP ready?

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...
Switzerland’s Parliament Moves to Accept FDA approved Medical Devices

Switzerland’s Parliament Moves to Accept FDA approved Medical Devices

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...
How to advertise your medical devices in the UK and avoid enforcement.

How to advertise your medical devices in the UK and avoid enforcement.

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...
Have you appointed the right UKRP? Part 3

Have you appointed the right UKRP? Part 3

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...
Have you appointed the right UKRP? Part 3

Have you appointed the right UKRP? Part 2

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...
Have you appointed the right UKRP? Part 3

Have you appointed the right UKRP? – Part 1

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...
The Regulatory Framework in Switzerland – Ordinances and CH-REPs

The Regulatory Framework in Switzerland – Ordinances and CH-REPs

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...
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