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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Leicester business Unimed Procurement Services secured government-backed financing to help it deliver life-saving medical equipment around the world.
This paper examines health in Tanzania
This consultation aims to seek views on the possible introduction of regulations mandating the disclosure of industry payments to the healthcare sector.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
Guidance for UK companies on winning business from international aid and development projects.
An overview of government's programme to develop and manufacture new medicines, digital health products and medical technologies.
The government’s plan to support a thriving UK medtech sector and make sure the health and care system can reliably access safe, effective and innovative medical technologies to deliver the best outcomes for patients.
The CMA has completed its remittal into the private healthcare market and has brought article 22 of the 2014 Order into force.
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