GRS News

The Role of AI in Medical Devices: Shaping Digital Health through Regulation

5/9/2024

The EU AI Act is part of a broader package of policy measures, including the AI Innovation Package and the Coordinated Plan on AI, designed to support the development of trustworthy AI and position Europe as a global leader in this field.

Navigating the Red Tape - Discussing Regulatory updates for MedTech in the UK

21/8/2024

Join our exclusive webinar to gain expert insights and practical, actionable guidance on the evolving regulatory landscape.

Navigating Post-Brexit Compliance: Appointing a UK Responsible Person (UKRP)

11/7/2024

UK Responsible Person (UKRP)

It’s Coming Home - While it’s already home: The Resilience of the UK Life Sciences Industry Amid Global Competitions and Challenges

11/7/2024

While we hope and pray that it officially is ‘Coming Home’, our team want to highlight the success of what actually has ‘Come Home’ and how ‘Home’ is supporting the mission!

Understanding the Guiding Principles for Transparency in Machine Learning-Enabled Medical Devices (MLMDs)

28/6/2024

FDA, Health Canada, and the UK's MHRA have released a comprehensive set of guiding principles focused on transparency for MLMDs.

Cannabis-Based Products for Medicinal Use (CBPMs) in the UK: Regulatory Landscape and Support Services

11/6/2024

Cannabis-Based Products for Medicinal Use - Regulatory Landscape and Support Services

GRS x MedCity

24/5/2024

Our recent activity with industry peers and partners.

Global Regulatory Services Partners with Ambitious Essex Innovation Accelerator to Foster Innovation and Regulatory Compliance

1/5/2024

"We are thrilled to be part of the Ambitious Essex Innovation Accelerator and to contribute our expertise in regulatory compliance to this pioneering initiative,"

Call for CBD-based cosmetics manufacturers to provide data on the safety of ingredients used in cosmetic products.

21/3/2024

The Commission Needs You!

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.