Welcome to our new website! If this is the first time you are logging in on the new site, you will need to reset your password. Please contact us at raps@raps.org if you need assistance.
Your membership opens the door to free learning resources on demand. Check out the Member Knowledge Center for free webcasts, publications and online courses.
This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
| 28 September 2012 | By Louise Zornoza
The UK's National Institutes of Health and Clinical Excellence (NICE), the country's cost containment agency, has cleared the use of Boehringer Ingelheim's alteplase (Actilyse) for the treatment of acute ischaemic stroke by the National Health Service (NHS) in final guidance issued on 26 September.
The guidance recommends starting treatment as early as possible within 4.5 hours after onset of stroke symptoms, and after intracranial haemorrhage has been excluded by appropriate imaging techniques. Alteplase is a tissue plasminogen activator, an enzyme that degrades fibrin clots and helps restore blood flow through blocked arteries.
According to Professor Carole Longson, the Director of NICE's Health Technology Evaluation Centre, "Today's guidance recommending the use of alteplase within the extended time frame for which it is now licensed has the potential to have a significant impact on the treatment of thousands of patients." According to the UK Stroke Association, every year more than 130,000 people in England and Wales suffer a stroke.
Read more:
Read all Breaking News from RegLink
Tags: Boehringer Ingelheim, Stroke, NHS, guidance