Thursday 17 March 2016

The SCIO Concept: How to Conduct Cost-Effective Clinical Trials

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For the past 20 years, the cost of new drug 
development has risen at a rate that was 7.4% 
higher than inflation, and clinical trials bear 
responsibility for most of that increase. 


Don’t Make Common Mistakes in Clinical Strategy


by Dr. Candida Fratazzi M.D.

Founder/CEOBBCR Consulting 

(Boston Biotech Clinical Research)




The average cost of developing a new drug is notoriously high. In a study conducted through the Tufts Center for the Study of Drug Development in 2014, Dr. Henry G. Grabowski and Dr. Ronald W. Hansen concluded, “The estimated average pre-tax industry cost per new prescription drug approval (inclusive of failures and capital costs) is 2,558 million.” The story does not end here. For the past 20 years, the cost of new drug development has risen at a rate that was 7.4% higher than inflation, and clinical trials bear responsibility for most of that increase. However, the increasing cost of biomedical research is not reflected in an increase in the success rate of clinical development. Instead, it presents a major hindrance to innovation in the biotech industry, while the public must bear the brunt of the problems, absorbing the steep rise in the prices of drugs and medical devices. In order to boost the efficiency of the biotechnology industry, remove the burden of expensive drugs, and create life science products in line with the future of healthcare, we should be asking how best to modify the development process to make it cost-effective.  
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