IDs and Tighter Trials Registration for Subjects in India
This is my site Written by Alex on December 5, 2009 – 1:51 pm   

The government in India is considering a system by which subjects enrolled in clinical trials would be assigned biometric identification. Read full story here. The move is designed to cut down on abuses and ensure the data coming out of the decade-old clinical trials industry in India is accurate. It should also help make trials safer for the subjects. A biometric ID is akin to an iris scan or fingerprint and is next to impossible to fake. The idea is a compelling one for a country that is also making registration of CROs and clinical trials mandatory. Perhaps other developing countries seeking to build a credible clinical trials industry will follow this lead and take similar steps.

In other clinical trials news…

Pluristem Therapeutics Completes Phase I Clinical Trial For Critical Limb 
Trading Markets (press release)
Pluristem received Clinical Trial Application approval to conduct clinical trials with PLX-PAD by the Paul Ehrlich Institute, the German competent authority 
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Santarus Announces Completion of Enrollment in European Phase III Clinical
Welt Online
This is the first of two induction phase clinical trials being conducted as part of the budesonide MMX Phase III clinical program. Santarus and Cosmo expect 
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Agreement Covers Clinical Trials in Nebraska
WOWT
Patients who are facing diseases and considering enrolling in a clinical trial will now have one less thing to worry about. Who’s going to pay for the care? 
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Firms have to register with govt for clinical trials on humans
Livemint
Organisations conducting clinical trials on humans will soon have to register with the government to be able to carry out such studies as India looks to 
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President Reagan’s Son Advocates for Alzheimer’s Awareness
Voice of America
Try to get people, your family members into the clinical trials, going to clinicaltrials.gov and see atrial that best fits your family member or a friend 
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Clinical Trials Update: Dec. 3, 2009
Palm Beach Post
To participate in this 52-week study, candidates must be 40 or older and have moderate-to-severe COPD. This study will evaluate an investigational 
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Insurance plan for clinical trials
Omaha World-Herald
By Rick Ruggles A lawmaker, an insurance federation and physicians Thursday announced more reliable insurance coverage for patients in clinical trials
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Clinical Trial Participants Are There Willingly
MedPage Today
By Crystal Phend, Senior Staff Writer, MedPage Today Explain to interested patients that ethical conduct of research, including clinical trials
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VIA Pharmaceuticals Completes Patient Visits in Phase 2 Trial of VIA-2291
PR Newswire (press release)
Completion of the data analysis and presentation of clinical trial results are anticipated in early 2010. VIA Pharmaceuticals, Inc. is a biotechnology 
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