I would like to announce about this workshop on behalf of patients and Doctors.As you know Clinical Research is being the most Important for the life expectancy but at the same time We do not want to do the Research in an unethical Way.This workshop will help the Doctors to Participate in Clinical Trial ethically and eventually benefits come to the Patients and to the World as such.
Cliniminds www.cliniminds.com, announced today one more ICH-GCP workshop to be held on 15th -16th November 2008 after getting huge response from previous workshops.
"These short term training programs are quite helpful for the professionals and students in the clinical research field,who can't attend regular training programs in clinical research",said Dr. Sood,Medical Director,Cliniminds.
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: 15th-16hth November 2008 (Saturday & Sunday)
Timings: 9 a.m. to 5 p.m.
Last Date of Registration: 10th November 2008.
Number of Seats: 15
Registration Fee: Rs.6000/- for working executives; Rs.3,000 for students.
Spot registration can also be done (subject to availability of seats)
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
Cliniminds www.cliniminds.com, announced today one more ICH-GCP workshop to be held on 15th -16th November 2008 after getting huge response from previous workshops.
"These short term training programs are quite helpful for the professionals and students in the clinical research field,who can't attend regular training programs in clinical research",said Dr. Sood,Medical Director,Cliniminds.
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: 15th-16hth November 2008 (Saturday & Sunday)
Timings: 9 a.m. to 5 p.m.
Last Date of Registration: 10th November 2008.
Number of Seats: 15
Registration Fee: Rs.6000/- for working executives; Rs.3,000 for students.
Spot registration can also be done (subject to availability of seats)
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