Nature Reviews Drug Discovery, Volume 13 2014 doi:10.1038/nrd4245
Yazı, 2001 Avrupa Direktifinin başarılı olamamasının ardından Avrupa'da klinik araştırmaların azaldığını ve yeni yasanın bu sıkıntıları aşmayı amaçladığını belirtiyor.
European parliament reaches provisional agreement on new rules for clinical trial authorization procedures.
The lowdown: The European Clinical Trials Directive was introduced in 2001 to harmonize clinical trial authorization procedures across Europe, but it failed miserably and is thought to have contributed to a decline in the number of trials carried out in Europe (trials fell by 25% from 2007 to 2011, according to one analysis). In a bid to fix an overly bureaucratic and slow process, the European Commission unveiled a new regulation in July 2012 to streamline clinical trial authorization (Nature Rev. Drug Discov. 11, 660?661; 2012). After a year and a half of negotiations with stakeholders, the European Union's Permanent Representatives Committee has approved a compromise agreement.
The regulation smoothes the trial application process such that sponsors will submit their trial requests through a single portal. A single authorization procedure will also be put in place across all EU member states. Under the terms of the compromise, trial applications for standard therapies must be reviewed within 60 days, and applications for complex medicinal products must be reviewed within 110 days. These are up from original proposed review deadlines of 48?79 days. Companies will also have to submit the results of all European studies to a publicly accessible database, a move brought on by calls for greater transparency in drug development.
The agreement now needs to be authorized by the Council of Ministers and the European Parliament plenary, and could be finalized before May.Shifts in industry, rather than public, investments are driving changes in the regional biomedical R&D landscape.
The lowdown: Justin Chakma, a venture capital investor at Thomas, McNerney & Partners in La Jolla, California, and his colleagues obtained data on biomedical research and development (R&D) expenditure in the United States, Europe and Asia-Oceania to look at spending trends between 2007 and 2012 (N. Engl. J. Med. 370, 3?6; 2014). While inflation-adjusted expenditure was stable over 5 years, increasing by only US$6.3 billion (2.4%) to $268 billion in 2012, the regional balance of biomedical research funding is changing (see figure).
Biomedical spending in the United States accounted for only 45.4% of the global R&D spend in 2012, when adjusted for purchasing-power parity, down from 51.2% 5 years prior, they report. ?The decline is remarkable because the United States has provided a majority of the funding for biomedical R&D globally for the past two decades ? a share that some previous analyses suggested was as high as 70 to 80%,? the authors write. Overall, the compound annual growth rate of biomedical spending from 2007 to 2012 in the United States was ?1.9%. Other regions that experienced a fall in compound annual growth rates were Europe, of ?0.4%, and Canada, of ?2.6%.