Written Questions are submitted by MPs or Lords to receive information from a Department.
|28 May 2020, 12:53 p.m.||Lord Kennedy of Southwark (Labour - Life peer)||Lord Kennedy of Southwark (Labour - Life peer)|
Question to the Department of Health and Social Care
To ask Her Majesty's Government what steps they have taken to streamline (1) legislative, or (2) regulatory, hurdles in the approvals process for treatments for COVID-19; and what safeguards will be built into any proposed changes to this process.
Answer (Lord Bethell)
The Medicines and Healthcare products Regulatory Agency (MHRA) is providing expedited scientific advice, and rapid reviews of clinical trials applications to support manufacturers and researchers on potential treatments for COVID-19.
The MHRA is also working closely with the Department and other healthcare partners and stakeholders to rapidly identify where flexibilities in the regulation of medicines and medical devices may be possible. This is with a view to supporting the healthcare products supply chain and wider response to the COVID-19 outbreak in the United Kingdom. These flexibilities are being offered to provide flexibility in exceptional circumstances. The flexibilities are temporary and will be kept under review, except where regulatory extensions have been stated.