Event:
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The Clinical Trial Study Protocol (Advanced)
- Hosted By:
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ComplianceOnline
- Start:
- Friday - Feb 22, 2013 10:00 AM
- End Time:
- Friday - Feb 22, 2013 11:15 AM
- Location:
- Online
- This clinical study protocol training will discuss the key elements in a study protocol and help you ensure that your protocol is clearly defined and conforms to GDA GCP guidelines.
Why Should You Attend:
Study protocols are an essential component of Good Clinical Practice (GCP) regulations.
In a clinical trial, the protocol is carefully designed to safeguard the health of the participants as well as answer specific research questions. A protocol describes what types of people may participate in the trial; the schedule of tests, procedures, medications, and dosages; and the length of the study.
This session will train investigators and clinical research staff in the key elements of a clinical study protocol, the process of protocol development and the specifics of FDA obligations to help ensure data integrity and institutional compliance.
- Website:
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Visit the website for detail info