10/7/2016

Date: October 13, 2016

Time: 11:00 am EST | 15:00 GMT

For more information: http://tinyurl.com/econsentwebinar

Our own SAM Sather and Mika Lindroos from CRF Health will discuss the important topic of regulatory risks in the informed consent process on this upcoming webinar. As you know, Informed Consent is one of the most cited GCP deficiencies by regulatory authorities and contributes to increases in the risk of delayed approvals, litigation and yes, even trial failure.

Join our webinar, 3 Major Regulatory Risks You Can Reduce with Electronic Informed Consent, to learn how new technological advances can help dramatically reduce these risks in your consent process.

To sign up click here.

Thank you!

-The Clinical Pathways Team