A person, who is independent of the trial, who cannot be unfairly influenced by people involved with the trial, who attends the informed consent process if the subject or the subject’s legally acceptable representative cannot read, and who reads the informed consent form and any other written information supplied to the subject.
Clinnovo offers services and training in clinical research course, clinical data management training, SAS, Imaging, Pharmacovigilance and drug regulatory affairs.
For more details please contact – http://www.clinnovo.com
Phone: 040-64635501 or 9912868928
Email: contact@clinnovo.com
Plot No: 4, Survey No:11/2,
Khanamet, Opp to Shilpa Ramam,
HitechCity,
Hyderabad – 81
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