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Medical Device Field Safety Corrective Actions

Medical Device Field Safety Corrective Actions

by Tim Bubb | Jan 18, 2023 | IMed Consultancy, Medtech Marketing

Medical Device Field Safety Corrective Actions STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe EU lay of the land  Medical devices, like all products can potentially go wrong. Robust processes...
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...
IVDR Transition and Notified Bodies…… Early engagement is still critical!

IVDR Transition and Notified Bodies…… Early engagement is still critical!

by Jonathan Ripley | Dec 1, 2022 | Academy, Clinical Writing, IMed Consultancy, IVD, MDR, Medtech Marketing

IVDR Transition and Notified Bodies…… Early engagement is still critical! 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...
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...
IVDR Transition and Significant Change…… What’s a Significant Change?

IVDR Transition and Significant Change…… What’s a Significant Change?

by Jonathan Ripley | Nov 30, 2022 | Clinical Writing, IMed Consultancy, IVD, MDR, Medtech Marketing, PMS

IVDR Transition and Significant Change…… What’s a Significant Change? STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe Regulation (EU) 2017/746, IVDR, is in place, and the market is in a 2nd...
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...
Alternative non-dilutive funding options for MedTech in the UK

Alternative non-dilutive funding options for MedTech in the UK

by Ellie Mills | Nov 30, 2022 | IMed Consultancy, IVD, MDR, Medtech Marketing, PMS, UKRP

Alternative non-dilutive funding options for MedTech in the UK STAY IN THE KNOW Sign up to get the latest updates. Don't worry.... we don't like spam either Success! Name Email Subscribe MedTech SMEs and startups often look to equity financing and other traditional...
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