Clinical Trial Data Rights?Comments on: -- http://e-patients.net/archives/2009/10/clinical-trial-data-rights.html because health professionals can't do it alone Sat, 11 Feb 2012 08:53:56 +0000 hourly 1 By: Nayan http://e-patients.net/archives/2009/10/clinical-trial-data-rights.html/comment-page-1#comment-74725 Nayan Wed, 02 Mar 2011 11:17:12 +0000 http://e-patients.net/?p=3618#comment-74725 Me and my colleagues authored one of India's most extensive reports on clinical trials. Drop me a mail if you are interested in a copy. My email is ntaluk@gmail.com. Some of the topics we included are: - Market Trends - Growth Drivers - Regulatory Bodies and Framework - Major Players. -Etc. We interviewed over 200 individuals and firms to collect the data in what we believe is one of the most detailed study on the subject in India. Nayan ntaluk@gmail.com Me and my colleagues authored one of India’s most extensive reports on clinical trials. Drop me a mail if you are interested in a copy. My email is ntaluk@gmail.com.

Some of the topics we included are:

- Market Trends
- Growth Drivers
- Regulatory Bodies and Framework
- Major Players.
-Etc.
We interviewed over 200 individuals and firms to collect the data in what we believe is one of the most detailed study on the subject in India.

Nayan
ntaluk@gmail.com

]]> By: Susannah Fox http://e-patients.net/archives/2009/10/clinical-trial-data-rights.html/comment-page-1#comment-48622 Susannah Fox Sat, 14 Nov 2009 15:27:07 +0000 http://e-patients.net/?p=3618#comment-48622 The following comment on this post was emailed to me by Ida Sim, MD, PhD, Associate Professor of Medicine and Director, Center for Clinical and Translational Informatics, UCSF. I am posting it with her permission: I led the WHO's International Clinical Trials Registry Platform (<a href="http://www.who.int/ictrp" target="blank" rel="nofollow">www.who.int/ictrp</a>) in 2005-6, and established global data and policy standards for trial registration to improve the transparency of clinical trial data reporting. That's still a strong underlying principle of my work - high-quality, open, and useful clinical research of real people in real life to improve health. The following comment on this post was emailed to me by Ida Sim, MD, PhD, Associate Professor of Medicine and Director, Center for Clinical and Translational Informatics, UCSF. I am posting it with her permission:

I led the WHO’s International Clinical Trials Registry Platform (http://www.who.int/ictrp) in 2005-6, and established global data and policy standards for trial registration to improve the transparency of clinical trial data reporting. That’s still a strong underlying principle of my work – high-quality, open, and useful clinical research of real people in real life to improve health.

]]> By: L Copen ill ministry http://e-patients.net/archives/2009/10/clinical-trial-data-rights.html/comment-page-1#comment-55738 L Copen ill ministry Sat, 31 Oct 2009 01:35:22 +0000 http://e-patients.net/?p=3618#comment-55738 <span class="topsy_trackback_comment"><span class="topsy_twitter_username"><span class="topsy_trackback_content">Clinical Trial Data Rights? | e-Patients.net http://ow.ly/xp0o</span></span> Clinical Trial Data Rights? | e-Patients.net http://ow.ly/xp0o

]]> By: Lodewijk Bos http://e-patients.net/archives/2009/10/clinical-trial-data-rights.html/comment-page-1#comment-48432 Lodewijk Bos Thu, 29 Oct 2009 20:36:56 +0000 http://e-patients.net/?p=3618#comment-48432 If I read this correctly, not even consent was given? If so, this is a gotspe. If I read this correctly, not even consent was given?
If so, this is a gotspe.

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