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Event Details
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
Who Will Benefit:
- Nursing staff
- Physicians
- Pharmacists
- Lab Technicians
- Finance/Accounting
- IT
- Marketing personnel
- Compliance officers
- Documentation personnel
For Registration:
When & Where
Online Webinar
2600 E. Bayshore Road
Palo Alto,
CA 94303
Friday, February 22, 2013 from 10:00 AM to 11:15 AM (PST)
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