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The UK unveils a new roadmap for medical device regulations.

15/1/2024

The Medicines and Healthcare products Regulatory Agency (MHRA) published a roadmap on Tuesday (09/01/2024), outlining the steps to implement new regulations for medical devices, including artificial intelligence, software, and diagnostics.

ECDRP replaced by IRP in the UK

2/1/2024

A very positive step post-Brexit providing a foundation for the MHRA to partner with other trusted global regulators and speed up the process of giving UK patients access to new life-saving medicines.

Launchpad: life and health sciences, Northern Ireland

7/11/2023

Are you a MedTech manufacturer looking to create new devices that can improve the lives and health of people? If so, you might be interested in a new funding opportunity from Innovate UK.

70 MG to 10 MG - what has changed for the CBD market in the UK?

12/10/2023

Important update for CBD product manufacturers selling product at > 98% purity (isolates).

IDAP Regulatory Support

19/9/2023

The Innovative Devices Access Pathway (IDAP) is a pilot initiative aimed at bringing new technologies and solutions to the National Health Service (NHS) to address unmet medical needs.

Horizon Europe UK

8/9/2023

UK joins Horizon Europe under a new bespoke deal

Medical Device Regulations 2023 – UK Amendments

21/6/2023

An attempt to continue providing essential medical devices to the patients.

GRS - Acing Global Excellence

27/3/2023

Global Regulatory Services (GRS) Awarded Global Excellence Award by Acquisition International

Intended Purpose for SaMD.

22/3/2023

Are you developing a Software as a Medical Device? This update is for you!

UK Budget 2023 Life science

15/3/2023

Scoop through important aspects of this budget for the Life science Industry.

GRS Family Expansion

30/1/2023

Welcoming our new Team Members!

Funding competition Fast Start Innovation

12/7/2022

UK registered small and micro businesses can apply for a share of up to £30 million for affordable, adoptable and investable innovations in net zero and Healthcare.

Government Publishes Consultation Response on the Future Regulation of Medical Devices in the UK

27/6/2022

Government Publishes Consultation Response on the Future Regulation of Medical Devices in the UK.

Regulatory Funding Opportunity for Health Tech SMEs

1/3/2022

If you are an SME working in HealthTech, you can apply for up to £30,000 of funding for use with regulatory affairs providers, to help you navigate regulatory pathways.

GRS are Best Healthcare Regulatory & Compliance Specialists 2020 - UK

29/12/2020

Global Health & Pharma Magazine has nominated Global Regulatory Services as the "Best Healthcare Regulatory & Compliance Specialists 2020 - UK". Naturally, we're delighted!

Webinar: Food Supplements Special Interest Group (SIG)-CBD and the latest developments

12/10/2020

Save the date: Join Medilink online on Thursday 29th October 2020 @ 11:00 to 12:00 and find out what's happening in the CBD ingestibles industry.

Webinar on 30th September 2020 - UK MedTech: how to keep your Device and IVD on the EU Market from Jan 2021

18/9/2020

In just over 3 months Brexit will happen. Are UK MedTech manufacturers ready? This webinar on Wednesday 30th September (11:00 to 12:00) will highlight challenges and provide solutions. By investing one hour of your time, you could well be securing the future success of your company in Europe.

UK CBD Pathway Clear As EU Decides

28/8/2020

HBW Insight interviews Greer Deal, Director of Global Regulatory Services about the latest events affecting the CBD Industry

Webinar on 15th September 2020: CBD - Where are we now and what's next?

20/8/2020

Save the date: Tuesday 15th September 2020, 12:00 to 12:45, GRS and Memery Crystal are hosting a webinar focused on CBD Novel Foods regulation, cutting through misinformation and fake news.

CBD in Europe: novel food or narcotic? What can companies do? Look to the UK!

19/7/2020

The European Commission (representing all the Member States) announced in January 2019 that CBD was a novel food. Since then CBD companies have been beavering away, gathering data and conducting toxicity and stability studies to compile their Novel Food Application dossiers for submission to the Eu...

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