The ICF Process: Tips on Achieving Optimal compliance and Comprehension
September 22, 2010(Ended)
Online Webinar
This ICF process Webinar training teaches how to create an informed consent process for achieving optimal site compliance and subject comprehension. It also discusses how an inadequate ICF can affect data integrity and patient safety and/or well-being.Areas Covered in the Seminar:
- The definition of the “Informed Consent Process” per regulations.
- The ethical standards surrounding the informed consent process .
- The roles of parties responsible for an adequate ICF process per FDA regulations.
- Barriers that affect subjects’ comprehension to the essential elements of the Informed Consent.
- The most common deficiencies noted in the Informed consent Process.
- The effects and consequences of an “inadequate” informed consent process.
- Tips on how to achieve site compliance and ensure subject comprehension to the ICF process.
This webinar will provide valuable information to personnel in Sponsor Companies (i.e., Pharmaceutical, Biotechnology, Medical Device, etc.) as well as CROs and investigator sites conducting clinical trials including:
- Clinical Research Associates
- Study Managers
- Site Staff/ Study Coordinators
- Clinical Investigators
Prices *
199 US Dollar
Exhibition
No exhibition
Organization
Categories
Concurrent events
- Why Medical Device Companies Receive Warning Letters - Webinar by GlobalCompliancePanel 2010
- The Cosmetic-Cosmeceutical Distinction: Walking the Line in Developing Label Claims - Webinar by GlobalCompliancePanel 2010
- Preparing for FDA Inspections in a Changing Regulatory Environment - Webinar by GlobalCompliancePanel 2010
- Compiling the Design History File, and Technical File / Design Dossier - Webinar by GlobalCompliancePanel 2010
- Project Management Certification Study Group - Information Year 2010
Important
Please, check the conference website for possible changes, before you make any traveling
arrangements
* Prices are for evaluation only.
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