Our knowledgeable Quality Manager Alan Yeomans is once again invited by eClinical Forum to host a webinar to an audience around the world. The webinar is called Requirements for Electronic Data for Regulated Clinical Trials (eCF Requirements) and will be offered twice: March 27th and then again on April 17.
Alan has over 30 years in the industry and has been a speaker at many of the top industry events like eClinical Forum, DIA and CDISC around the world.
Alan has been at the company for 10 years and through the years he has been an essential contributor to the development of Viedoc. Lately, he has supported the Viedoc team on GDPR compliance. Viedoc customers can trust they are using a system that complies with all industry regulations allowing them to concentrate on what they do best!
Viedoc - Enjoy your trial!
"Viedoc makes building a study easy and fun. It doesn't require extensive coding knowledge; it's quick to get in and start working."