Re-Posted from eCF LinkedIn Group
The FDA and OHRP published final guidance aimed at providing answers to commonly asked questions about using electronic systems and processes that may employ multiple electronic media to obtain informed consent. Expand the article to read more
The eCF EDC Hosting Team has released the final White Paper documenting best practices for establishing controls and operational procedures that facilitate compliance with evolving regulatory expectations for Electronic Data Capture in Clinical Trials using Service Providers. Expand the article to read more and to access the documents.
Time: UTC 1500; 16:00 CET, 10:00 AM EST, 11:00 PM Singapore. We apologize for the inconvenient timeslot in some regions.
Facilitator: Michelle Flickinger, Array Biopharma;
Open To: Staff from eClinical Forum member companies, gratis.
eCF Birds-of-a-Feather sessions focus on the details of a specific topic and are participative discussions, not presentations. All participants are encouraged to share information and ask questions. Click for more information...
We had a fabulous level of participation with well over 50 members online from California to Japan participating in our Technology Showcase exploring electronic informed consent and demonstrating Enforme Interactive/Drug Dev’s SecureConsent Application for eICF. Some good discussion helped us to understand the business opportunities and value. Materials are available for download. Expand the article to read more about the event.
Electronic Informed Consent in clinical trials has been highlighted as a topic of interest at recent eClinical Forum meetings. The technology demonstration will provide an insight into the functional capabilities of the Enforme system and will discuss the practical implementation of such systems.
Time: UTC 1400; 15:00 CET, 09:00 AM EST, 10:00 PM Singapore. Registration: https://www.surveymonkey.com/r/eCF_TS_eICF