Looks like this event has already ended.
Check out upcoming events by this organizer, or organize your very own event.
The Clinical Trial Study Protocol (Advanced)
Friday, February 22, 2013 from 10:00 AM to 11:15 AM (PST)
Palo Alto, CA
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
- Lab Technicians
- Marketing personnel
- Compliance officers
- Documentation personnel
When & Where
At ComplianceOnline, we are focused on :
- Enhancing global compliance, creating a world where quality and compliance professionals, regulators, and government agencies come together to help the world comply with the intent and the spirit of laws, policies and mandates, ensuring continuous improvement in global operations, quality & safety.
- Making sure that we are responsible corporate citizens helping our constituents build a more responsible enterprise, one which operates with high quality , under a code of ethics, and with process discipline to ensure greater shareholder returns.
- Keeping things simple and straight forward , so that we all can indeed improve the quality of our processes, our work, our businesses and enhance compliance globally.
- Being inclusive, giving the process experts ( & novices! ), compliance professionals, quality champions, and regulatory agencies a voice so that all of us can contribute and make a difference.