The Clinical Trial Study Protocol (Advanced)

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.

Areas Covered in the Webinar:

• The “Key” Document
• Study details as well as the purpose, goals, potential issues, and more
• Elements of study protocol
• GCP Guidelines for a Study Protocol

For Registration:

http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702746?channel=worldconf