CardiovascularChairs Re-appointed To The Commission On Human Medicines And The Herbal Medicines Advisory Committee
The Medicines and Healthcare products Regulatory Agency (MHRA) and the Appointments Commission are pleased to announce the re-appointment of the chairs to both the Commission on Human Medicines (CHM), and the Herbal Medicines Advisory Committee (HMAC).
Sir Gordon Duff has been re-appointed as chair of the CHM and has served on the committee for the past 16 years. He received a knighthood for services to public health in 2006.
Currently the Florey professor of molecular medicine at Sheffield University, he also chairs the Scientific Pandemic Influenza advisory committee and is co-chairman on the Scientific Advisory Group for Emergencies.
Sir Gordon has previously served as chairman of the National Biological Standards Board (NBSB) and chairman of the secretary of state"s expert scientific group on phase one clinical trials.
He is an honorary fellow of the faculty of pharmaceutical medicine of the Royal College of Physicians as well as being a fellow of the Royal College of Physicians (London and Edinburgh), the Royal Society of Edinburgh and the Academy of Medical Sciences.
His research interest is in the immunology and genetics of inflammatory diseases.
Professor Philip Routledge OBE has been re-appointed as chair of the HMAC. He is currently head of the department of pharmacology, radiology and oncology at the Wales College of Medicine at Cardiff University and is chair of the All Wales Medicines Strategy Group (AWMSG), a public appointment in Wales.
He is an honorary consultant physician and clinical pharmacologist at the Cardiff and Vale NHS Trust. Professor Routledge trained at the University of Newcastle in general medicine and clinical pharmacy.
The CHM and the HMAC advise UK health ministers on the regulation of medicines and on traditional herbal medicines respectively. These independent bodies work closely with the MHRA.
Both appointments are for a four year term commencing 31 October 2009 and are not remunerated. However, a fee of ÷£400 per meeting is paid to cover preparation and attendance together with any travel and accommodation costs.
All appointments are made on merit. Political activity plays no part in the selection process. In accordance with the original Nolan recommendations there is a requirement for appointees" political activity (if declared) to be made public. Philip Routledge has declared membership to the Liberal Democrats.
The appointments were made in accordance with the Commissioner for Public Appointments Code of Practice.
Notes
1. Sir Gordon Duff graduated in medicine from St Peter"s College, Oxford, and St Thomas" Hospital Medical School in London, where he also undertook a PhD in the neuropharmacology of fever. After postgraduate medical training including clinical pharmacology at Hammersmith Hospital, he worked in the infectious disease section at Yale Medical School (USA). He also worked in the rheumatology department at Edinburgh University before taking up his present post as Florey professor of molecular medicine at Sheffield University. Sir Gordon was chairman of the NBSB from 2002 to 2009 and of the secretary of state"s expert scientific group on phase one clinical trials in 2006. He served on the CHM and its predecessor, the Committee on Safety of Medicines, since 1993.
2. Professor Philip Routledge OBE qualified in medicine from the University of Newcastle upon Tyne in 1972. He trained in general medicine and clinical pharmacology both there, and in the USA. In 1981, he joined the Welsh National School of Medicine (now Wales College of Medicine, Cardiff University).
3. Details of the Commission on Human Medicines can be found at:
Commission on Human Medicines
4. Details of the Herbal Medicines Advisory Committee can be found at:
Herbal Medicines Advisory Committee
5. Details of the Appointments Commission is available on their website:
Appointments Commission (external link)
6. Details of the Nolan Recommendations can be found on the Commissioner for Public Appointments website
Commissioner for Public Appointments (external link)
7. The MHRA is the government agency responsible for ensuring that medicines and medical devices work, and are acceptably safe. No product is risk-free. Underpinning all our work lie robust and fact-based judgements to ensure that the benefits to patients and the public justify the risks. We keep watch over medicines and devices, and take any necessary action to protect the public promptly if there is a problem. We encourage everyone - the public and healthcare professionals as well as the industry - to tell us about any problems with a medicine or medical device, so that we can investigate and take any necessary action.
Medicines and Healthcare products Regulatory Agency