Webinars, Seminars and Demonstrations
SureClinical’s webinars help you to learn best practices on how leading organizations are implementing cloud-based electronic trial master file solutions, and easy it is to reduce manual paper-based processes in clinical trial studies. See how companies are reducing or eliminating document printing and scanning using Adobe PDF digital signing within an FDA and EC compliance validated environment. Quantify the cost savings of moving from paper-based processes to automated processes with SureClinical eTMF. Contact us today to learn more about webinars and demonstrations.
Webinar: Go Digital with SureClinical Cloud
Seminar date: Thurs 1 October 2015 3:00PM – 4:00PM UK Time
Online Registration: SureClinical Webinar Details and Registration
Learn how clinical research organizations and sponsors are leveraging the power of cloud-based Electronic Trial Master File solutions and digital signing to eliminate paper, save time and simplify clinical trial document management.
In this seminar you will learn best practices for implementing an eTMF within a clinical study team of remote study team members and investigators, and how study teams can manage their documents from the office and on the go. Study startup is accelerated through the use of templates, while study documents can be electronically uploaded and signed. SureClinical offers a safe and secure cloud platform, audited for compliance against FDA 21 CFR Part 11 and EC Good Manufacturing Practice Annex 11.
“Before SureClinical, DNAtrix managed most of its regulatory documents on paper. We now have the flexibility to securely share and e-sign documents with clinical trial personnel anywhere in the world.”
– -Sheri Forsythe, Director, Clinical Trial Operations, DNAtrix
“This seminar will bring together industry experts to discuss real-world deployment of eTMF applications and eTMF data standards, and how eTMF applications can be used to improve clinical trial operational efficiencies, collaboration and data sharing between sponsors, clinical research organizations, investigators and clinical trial stakeholders,” said Lou Chappuie, COO, SureClinical.
Clinical Research Organization SterlingBio will share their criteria for selecting an eTMF solution, experience and best practices for the elimination of paper, including how to deploy digital signatures to clinical investigator sites and the business benefits of eTMF data standards.
Register today for the webinar to learn from these experts:
-Lou Chappuie, Chief Operating Officer, SureClinical; Member, OASIS eTMF Standard Technical Committee
3:00 PM: Intro and SureClinical Overview
3:20 PM: SureClinical eTMF Demo
3:40 PM: Best practices in implementing a cloud eTMF / Q & A
To register for the free seminar visit: SureClinical Seminar Registration
This event is for professionals in the biopharma industry. SureClinical reserves the right to confirm your attendance and legitimate interest in attending this informative seminar. All registered attendees will be verified upon check-in.
Have questions? Contact us at 916-265-2000 (California USA)