The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has launched a public consultation seeking input on its proposals for in-house manufacturing of medical devices. As healthcare providers increasingly explore on-site production to meet patient needs and improve service delivery, the MHRA aims to establish clear regulatory frameworks to ensure safety and compliance. This move marks a significant step in the evolving landscape of medical device regulation within the United Kingdom, with stakeholders across the industry invited to contribute their views.
UK’s MHRA Invites Industry Input on In-House Device Manufacturing Practices
The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) is actively seeking input from medical device manufacturers regarding current practices surrounding the in-house production of devices. This call for feedback aims to harmonize standards and ensure patient safety and regulatory compliance amid a growing trend of…
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Author : Atticus Reed
Publish date : 2025-08-16 04:25:00
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