Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
BMJ 2003;326:1220 (31 May), doi:10.1136/bmj.326.7400.1220-a
| The first 150 words of the full text of this article appear below. |
There is evidence that industry sponsored research leads more often to an outcome favourable to the drug under investigation (p 1167). Studies with low methodological quality tend to overestimate an effect but the methodological quality of studies funded by drug companies is no worse than that of other studiesoften it is even better.
Developing new drugs without the industry is unfortunately not realistic.
Let's ignore all the preclinical researchthis is regulated by good
laboratory practice guidelines
(www.oecd.org/env/glp).
Let's jump directly to clinical research. Good clinical practice (GCP)
protects research subjects and is a quality assurance tool. The International
Conference on Harmonisation of Technical Requirements for Registration of
Pharmaceuticals for Human Use (ICH) "is a unique project that brings
together the regulatory authorities of Europe, Japan, and the United States
and experts from the pharmaceutical industry in the three regions to discuss
scientific and technical aspects of
Marcus Müllner1
1 BMJ marcus.muellner@univie.ac.at
Read all Rapid Responses
What can you learn from this BMJ paper? Read Leanne Tite's Paper+