ICH - GCP Clinical Research Workshop
Saturday 9th & Sunday 10 February 2008, New Delhi
This workshop has been developed to provide 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: 9th-10h February 2008 (Saturday & Sunday) - Timings: 9 a.m. to 5 p.m.
Last Date of Registration: 5th February 2008. Limited seats available.
Registration Fee: Rs.4,500/- for working executives; Rs.3,500 for students ;Rs.2000/- for Cliniminds students
Payment Mode: By Cash or Bank Draft/Cheque favoring ‘Tenet Health Edutech Pvt. Ltd., payable at New Delhi. You can also make payment by Credit Card through our website – www.cliniminds.com
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
Cliniminds
C-55 First Floor, Preet Vihar,
Main Vikas Marg, Delhi 110092; Mobile: 9871072560; 9810068241
Email: info@cliniminds.com; Website: www.cliniminds.com
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