Fundamentals of Clinical Research - Key players and roles for a successful and compliant research te (Clinical Compliance )

Venue: Online Event

Location: Palo Alto, California, United States

Event Date/Time: Dec 06, 2011 End Date/Time: Dec 06, 2011
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The presenter will provide practical tips on how to work with the research team of other professionals to help with a successful outcome while maintaining integrity of the trial. This session will include the key principles of GCP as defined by the ICH as well as incorporate FDA regulatory inspection strategy to identify areas of common deficiency.

Areas Covered in the Seminar:

- ICH guidelines and Good Clinical Practice (GCP).
- Types and Phases of Clinical Trials.
- Role and responsibilities of a Clinical Research coordinator.
- Key aspects of the role and key players involved in a trial.
- Role of the Principal Investigator.
- Activities that are common to most trials.
- Linking responsibility to these activities.
- Institutional Review Board/ Informed consent.
- Trial- from selection to closing.

NOTE : Use this Promocode (128600)to avail 10% discount,Valid till December 30 & add another webinar to your shopping cart and get 20% off on its price.


Online Event
2600 E. Bayshore Road
Palo Alto
United States