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And it ensures the safety and effectiveness of medicines in the UK. You can find out more in our naming of medicines guidance (PDF, 235 KB, 20 pages). An updated list of suspended licenses has been uploaded. PDF Guidance for UK Manufactur Licence and Manufactur - GOV.UK Updated content to reflect that the UK cannot act as a Reference Members State (RMS) for approval of marketing authorisations in decentralised and mutual recognition licensing procedures during the transition period. Updated the list of companies in the UK who have their licence to manufacture or wholesale medicines terminated and cancelled. Comment by Wed like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services. Well send you a link to a feedback form. New list of suspended manufacturing and wholesale distribution authorisations added to the page. Updated list of suspended licences added to the page. Read More Contract Manufacture NJ MVC | Suspensions and Restorations AL10 9UL, New September 2020 version of 'Medicines terminated, cancelled and revoked manufacturing and wholesale dealer licences'. Product Licences - UK MHRA, MCA and EMA | MPA Business Services What the data show Since September 2020, 15 Companies were affected. Cancellation of a licence, authorisation or registration is when MHRA makes a decision to cancel the licence, authorisation or registration. You have rejected additional cookies. MHRA Suspended Licence checks are a critical part of your Quality Management System and Risk Management processes, so keep on top of them. Ilyas ali We also use cookies set by other sites to help us deliver content from their services. Once we revoke your licence we cannot change our decision unless it is for one of the following reasons: You can appeal our decision to revoke your licence in a Magistrates or Sheriff Court. Refrain from driving for a period of time. This does not replace your right of appeal through the courts. These templates should not be altered in any way, other than inserting the relevant information. It is the MA applicants responsibility to make sure that the ASMF is submitted either before you submit your application or at the same time, as your application will not be valid without it. New list of suspended licenses added to the page. This blog shares the work of the Medicines and Healthcare products Regulatory Agency (MHRA) Inspectorate, by inspectors and those the Inspectorate works with. Following recent advice from the EMA, the MHRA have suspended all licenses for ranitidine products. If you do not respond to our letter we will revoke your licence automatically after 21 days.