CLINICAL COMPLIANCE 2011 - Ethics, Standards and Identifying Risks in Clinical Research

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CLINICAL COMPLIANCE 2011 - Ethics, Standards and Identifying Risks in Clinical Research - Clinical webinar By ComplianceOnline

Website http://complianceonline.com/ecommerce/control/trainingFocus/~product_id=701806?channel=ourglocal | Edit Freely

Category Clinical Webinar ,conference,event.

Deadline: January 20, 2011 | Date: January 20, 2011

Venue/Country: Palo Alto, U.S.A

Updated: 2010-12-03 17:32:13 (GMT+9)

Call For Papers - CFP

This clinical research ethics training will impart an understanding to regulatory compliance and clinical study personnel on the importance of ethics in clinical research and impart a familiarity with the regulations to protect both the researcher and the subject.

Areas Covered in the Seminar:

Overview of the main ethical principles to be considered in the development and conduct of research to protect both the researcher and the subject.

Responsibilities of

Research sponsors

Clinical researchers

Institutional Review Boards (IRBs)

Description of the standards and requirements of informed consent.

The role of drug safety committees.

Ethical and regulatory issues relating to

Tissue procurement

Stem cell research

Organ transplantation

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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