ICH – GCP Clinical Research Workshop on Saturday 12th & Sunday 13 January 2008 at New Delhi

Delhi, India, December 28, 2007 --(PR.com)-- This workshop has been developed to provide an overview of clinical research process with a comprehensive review of ICH GCP, USFDA CFR 21, Schedule Y and the elements involved in coordinating a clinical trial.

Who Should Attend?

• Medicine / Life Sciences / Science Graduates & Post Graduates & Students
• Entry level clinical research professionals with limited experience
• Anyone interested in the field of clinical research.

Following Sessions will be covered during the workshop by industry experts:

• Fundamentals of Clinical Research
• Ethical Concerns and Human Subject Protection
• Regulatory Issues
• Clinical Trial Documents
• Subject Recruitment & Retention
• Conduct of Clinical Trials
• Adverse Event Reporting

Course Objectives: Upon completion of the workshop, the attendee should be able to understand the clinical research fundamentals, conduct and management of clinical trials, ethical issues and regulatory issues.

Dates of Workshop: 12-13 January 2008 (Saturday & Sunday) - Timings: 9 a.m. to 5 p.m. Last Date of Registration: 8th January 2008. Limited seats available.

Registration Fee: Rs.4,500/- for working executives; Rs.3,500 for students

Payment Mode: By Cash or Bank Draft/Cheque favouring ‘Tenet Health Edutech Pvt. Ltd., payable at New Delhi.

Workshop Venue : Cliniminds, C-55 First Floor, Preet Vihar, Main Vikas Marg, Delhi 110092

Certificates: Certificates of Participation will be issued to all participants.

For Registration & Information Please Contact
C-55 First Floor, Preet Vihar,
Main Vikas Marg, Delhi 110092; Mobile: 9871072560; 9810068241; 9999851016; Email: info@cliniminds.com; Website: www.cliniminds.com

Suraj Shaw