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PHARMACEUTICAL INDUSTRY DIRECTORY

Health Protection Agency

Health Protection Agency

The Health Protection Agency is a national organisation which is dedicated to protecting people’s health and reducing the impact of infectious diseases, chemical, poisons and radiation hazards.  Formed in 2003 by bringing together expertise in various aspects of public health the Agency has three national Centres, a network of regional laboratories and over 3000 staff.

The Agency derives a significant proportion of its income from commercial activities which include : microbiological, chemical and radiological testing, research and development contracts, custom biopharmaceutical manufacture of biological products, consultancy and training, as well as products including diagnostic kits and therapeutic medicines.  The Agency has four culture collections supplying authenticated bacterial, fungal, viral and cell cultures on a global basis.

Core business areas include research and development of vaccines against infectious diseases, process development and GMP manufacture of biologics derived from microbial fermentation - particularly those requiring containment or focused on the bio-defence market.  As well as a wide range of services including biosafety, GLP immunoassay and vaccine testing, evaluation of diagnostic tests and in-vivo studies.

The Centre at Porton Down works to improve the UK's emergency response capability by developing the infrastructure for surveillance and early recognition of events. To improve preparedness we run training courses and co-ordinate emergency exercises to provide testing of emergency plans. We produce CBRN guidance for health professionals, as well as bio-security advice to UK, US and European governments and other agencies.

020 7759 2700
webteam@hpa.org.uk
www.hpa.org.uk
7th Floor, Holborn Gate, 330 High Holborn, London, WC1V 7PP
 
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Industry Events

4th Annual Patient Recruitment and Retention in Clinical Trials

13-15 October 2008, Amsterdam

Patient recruitment is now consuming thirty percent of clinical trial time - more time than any other clinical trial activity - and almost half of all trial delays result from patient recruitment problems. As the recruiting culture becomes more sophisticated and the forces affecting patient enrollment grow more numerous and complex, pharmaceutical companies are striving to discover new strategies to facilitate enrollment in clinical trials. With increasing industry pressure to develop, test and market greater numbers of new drugs faster, pharmaceutical companies need to perform clinical trials as quickly as possible. Inefficient patient recruitment processes is a formidable barrier to pharmaceutical companies' success in launching new products. Improving the patient recruitment process is imperative to avoid wasted investments and eliminate costly delays in bringing new drugs to market -- today and even more so in the not-so-distant future. Improved patient recruitment presents one of the largest opportunities for pharmaceutical companies to eliminate delays in clinical trials, thereby making it possible to reduce time to market.  With patent time limits and large overheads meaning that any delays in the development timeline can be disastrous, a good understanding of how to successfully recruit patients for trials is vital for any company looking to succeed.
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News and Press Releases

Biomedical Systems Names New Managing Director For European Headquarters

St. Louis, MO - Biomedical Systems, a global provider of centralized diagnostic services for clinical trials, announced that Geert Dewulf, MD has been named the Managing Director, European Operations. Dr. Dewulf will assume the top post in the company's European Headquarters in Brussels, Belgium from Rita Jacobs, who will be retiring from that post after 27 years with the organization. Dr. Dewulf came to Biomedical Systems from Agfa Healthcare where he served as Managing Director for Germany, Austria and Switzerland.
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