ARTICLE
19 October 2020

Update On The UK Medicines Regulator Post Brexit

JA
J A Kemp LLP

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J A Kemp is a leading firm of European Patent and Trade Mark Attorneys. We combine independent thinking with collective excellence in all that we do. The technical and legal knowledge that we apply to the protection of our clients’ patents is outstanding in its breadth and depth. With around 100 science and technology graduates in the firm, including 50 PhDs, no area of science or technology is outside our scope. Our Patent Attorneys have collective in-depth expertise in patent law and procedure in every country of the world. The team of professionals who advise our clients on trade mark and design matters have backgrounds in major international law firms and hold qualifications as Chartered UK Trade Mark Attorneys, Solicitors and European Trade Mark Professional Representatives. Dedicated to this specialist area of intellectual property protection, the team has the expertise and resources to protect trade marks and designs in any market worldwide.
The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has joined the Australia-Canada-Singapore-Switzerland (ACSS) Consortium, with effect from 1 January 2021.
United Kingdom Food, Drugs, Healthcare, Life Sciences

The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has joined the Australia-Canada-Singapore-Switzerland (ACSS) Consortium, with effect from 1 January 2021.

The group will be renamed as the Access Consortium to reflect the addition of the UK, which increases the combined population of the participating countries to approximately 145 million. Pharmaceutical companies that submit applications to some or all of the five Access countries may have their products evaluated for marketing in those countries simultaneously, with reduced evaluation times. Updated guidance to industry on how to apply for a product to be considered for marketing authorisation across the five member countries, including the UK, will be provided by the Consortium in due course.

The MHRA is one of the world's leading regulators of therapeutic products and it is to be hoped that membership of the well-established collaboration group will help to maintain this status, whilst also helping to ensure timely access to medicines in the UK and the other member countries. UK marketing authorisations secured by this route may be used by UK patent owners as the basis to apply for supplementary protection certificates covering the UK.

The content of this article is intended to provide a general guide to the subject matter. Specialist advice should be sought about your specific circumstances.

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