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Promising developments on early access to medicines in the UK

Promising developments on early access to medicines in the UK

This morning (21 January 2014) I attended the Empower Access to Medicines campaign meeting to discuss speeding up access to medicines for patients most in need.

It was great to hear Department of Health Minister Earl Howe’s thoughts on government’s plans for introducing an Early Access to Medicines scheme, which is something the BIA has long campaigned for.

I was particularly pleased to hear that government thinking was “at an advanced stage” with “active discussion across Whitehall” about the introduction of a new “promising innovation medicine” designation as part of their proposed scheme.

Earl Howe explained that the UK government recognises the success of “breakthrough therapy” designation in the United States over the past 18 months and hopes that the new UK designation would provide a similar boost for innovative therapies developed in the UK. We’ve seen the importance of “breakthrough therapy” designation at the FDA on investor sentiment and the speed of drug approval in the USA, so it would great for companies in our sector to see this real policy innovation from the UK government.

I think that such a “promising innovation medicine” designation would enable companies to signal in a straightforward way to potential patients and investors that they were adopting the speediest and most efficient regulatory process and had mapped-out and would utilise the most appropriate route to work with NHS centres of excellence and Academic Health Science Networks to ensure timely adoption and usage of a new therapy.

In addition to its potential to significantly accelerate designated treatments to those patients who need them, the designation is likely to have a positive effect on the companies developing the products and on the investment community’s perception of those companies.

I believe the “promising innovation medicine” designation could prove more valuable than the FDA’s “breakthrough therapy” designation because it is likely to be linked with a process that delivers reimbursement via an Early Access to Medicines scheme. Medicines receiving the “promising innovation medicine” designation will be on the fast track for the most efficient regulatory engagement with the MHRA using all the existing flexibilities available and then given VIP access into the NHS system through the appropriate centres of excellence.

The combination of the “promising innovation medicine” designation and an Early Access to Medicines scheme should enable NHS patients in the UK to be amongst the first in the world to benefit from new therapies and ensure the UK is a world leading location to start, build and develop the biotech companies that deliver such breakthroughs.

I have reason to be optimistic.


Steve Bates is CEO of the BioIndustry Association. This article orinally apeared on the BIA website


A full list of attendees can be found below. For more information about the meeting please contact James Hargrave on 0203 267 0074.


Dr Peter Feldschreiber, 4 New Square
Dr Martin Turner, AMRC
Stephen Whitehead, Association of British Pharmaceutical Industry
Professor Sir Peter Lachmann, Empower: Access to Medicine/Cambridge University
Professor Richard Barker, CASMI
Geoffrey Clifton-Brown MP, Cotswolds
Richard Carter, Department of Health
Emily Crossley, Duchenne Children’s Trust
James Hargrave, Empower: Access to Medicine
Jennifer Bryant-Pearson, Empower: Access to Medicine
Sir David Cooksey, Francis Crick Institute
Dr Louisa Petchey, Genetic Alliance UK
Earl Howe, Health Minister
Leela Barham, Independent Consultant
Dr Jack Scannel, Independent Consultant
Alex Johnson, Joining Jack
Dr Ian Hudson, MHRA
Gian Marco Currado, MHRA
John Kel,l MND Association
Claymore Richardson, Earl Howe's Private Office
Lucy Notridge, Earl Howe's Private Office
Dr Dougal Goodman, The Foundation for Science and Technology
Steve Bates UK, BioIndustry Association
Dr Jeremy Farrarm, Wellcome Trust


  • Our grandson aged 3 yrs has Duchenne’s MD & autism.
    We as a family are desperate for a treatment that may help our little one. Is a cure in his lifetime too much to hope for? My family also carries the Huntingtons gene. Are we to watch our grandson die, as we did my father, sister, cousins, uncles & grandparent?. I’ts about time we had the funding. Our Jay is an only child whose parents are to scared to have another child living with a death sentence hanging over it. We need this to go through. It may not be in time to help our little one but, we know many other families with children suffering these terrible diseases, & I am sure there are many more unborn babies yet to come, who will also suffer.

    Sheila Baldwin 10-02-14 6:59pm

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Please contact James Hargrave at JBP PR or telephone 0203 267 0074 for any press or event related enquiries.