Ethics, Standards and Identifying Risks in Clinical Research - Clinical Compliance Webinar By ComplianceOnline

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

Who Will Benefit:

Management teams in pharmaceutical development
Personnel involved in clinical trials within the pharmaceutical and biotechnology industries
Service providers supporting pharmaceutical and biotechnology industries

Note: Use these promocode(117660) for 10% discount.