Web Seminars for Clinical Research Professionals
A Barnett Interactive Web Seminar offers you a seamless, secure, multimedia learning experience. These live, instructor-led sessions are designed to be highly interactive, and can be attended by individual attendees or groups at one low cost. No travel, no travel expenses, and no time away from the office!
Informed Consent Guidance: Regulatory Updates
Conducting the informed consent process is one of the most critical tasks to be completed by a research site. It is essential that a subject clearly understand the language in the consent form and that their rights, safety and welfare are not jeopardized in any way. In this web seminar, we will look at the essential language in the informed consent document through review of the FDA regulations and guidance documents, including the “Guidance on Exculpatory Language in Informed Consent” and additional regulatory updates and considerations.
- Navigate the regulatory climate related to the new guideline: Why the guidance?
- Discuss the content of the guideline: What do you need to know?
- Present the implications of the guideline on current practices and policy: How does it impact how you conduct clinical trials?
- Research Site Managers
- Investigators
- Clinical Research Coordinators
- Clinical Research Associates
- Clinical Research Associate Managers
- Project Managers
- Sponsor/CRO Staff
- Clinical Quality Compliance and Quality Assurance Professionals
Nikki Christison, B.S.
Click here for complete trainer biographies
Hold this course at your company! For more information, contact Naila Ganatra at (215) 413-2471.
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