Market and patient access to new oncology products in Europe: a current, multidisciplinary perspective

Author:

McCabe C.,Bergmann L.,Bosanquet N.,Ellis M.,Enzmann H.,von Euler M.,Jönsson B.,Kallen K.-J.,Newling D.,Nüssler V.,Paschen B.,de Wilde R.,Wilking N.,Teale C.,Zwierzina H.

Publisher

Elsevier BV

Subject

Oncology,Hematology

Reference49 articles.

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2. Fourth hurdle reviews’, NICE, and database applications;Paul;Pharmacoepidemiol Drug Saf,2001

3. Inclusion of cost effectiveness in licensing requirements of new drugs: the fourth hurdle;Taylor;BMJ,2004

4. US Food and Drug Administration, Center for Biologics Evaluation and ResearchFrequently Asked Questions: What is a Biological Product? www.fda.gov/Cber/faq.htm#3 (25 April 2008, date last accessed)

5. Phase II study of rituximab plus fludarabine in patients with low grade lymphoma: final report;Czuczman;Blood,2001

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