EUCROF released a paper with proposals on the early publication of clinical trial information, balancing the public’s need for transparency and innovators’ intellectual property and confidentiality rights.
This paper has been prepared to outline the EUCROF’s position on specific aspects of the implementation of the EU Clinical Trials Regulation for early phase, non-paediatric, non-publicly funded clinical trials, performed in healthy volunteers or patients with the target disease…
Publish date: Nov 4, 2014
By: Philip Ward
