The below is an update from the MHRA – 15/06/2020 – on the Coronavirus situation

For more information on Coronavirus, click here

This notice updates you on details of recently published guidance for industry on the coronavirus (COVID-19) pandemic and how we are working closely with our healthcare partners to contribute to the essential global action needed to protect public health at this challenging time.

We would welcome your further feedback on what other information you would find useful – please email [email protected]

Regulatory flexibilities

We continue to work with stakeholders to develop, refine and publish updates to our regulatory flexibilities page. We have added information on audits of Notified Bodies and manufacturers in the medical devices section.

Other guidance for industry

New or updated guidance that we have published on our general guidance page for industry since the last edition of this email:

Details of guidance:
This guidance is on how to use the current regulatory flexibilities or how to get an exceptional use authorisation from MHRA for software or app intended specifically for the pandemic response.

Details of guidance:
We added Target Product Profiles (TPP) for Enzyme Immunoassay (EIA) antibody tests to help determine if people have antibodies to SARS-CoV-2.

Contacting the MHRA

Most of our workforce is working from home, although National Institute for Biological Standards and Control (NIBSC) is continuing essential laboratory activities on site. If you need to get in touch with us during this period, please email or phone us.

For more information please visit mhra.gov.uk

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