Patient consent is one of the most important parts of clinical trials, yet is consistently the number three critical finding from regulatory inspections resulting in an FDA Form 483. Why is this?
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Join us for a complimentary lunch and hands-on ICH E6(R2) workshop. Design an RBM implementation framework that can be utilized in your study or organization.
To learn more or to register for this workshop, please visit: Hands-on RBM workshop
OmniComm Systems and Tri-I Biotech have joined forces to bring together industry thought leaders and businesses to discuss the latest innovative strategies in the life sciences industry. We have created a dynamic agenda, to explore the evolving requirements of clinical trials and understand how the latest technology is rising to meet the challenges.
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May 10 Summit
OmniComm Systems is a proud sponsor of Outsourcing in Clinical Trials Europe - Booth #66.
Email firstname.lastname@example.org to schedule a meeting at OCT Europe with our team.
OmniComm Systems is a proud sponsor of the DIA Annual Meeting. Visit Booth #1823 to meet our executive team.
Email email@example.com to schedule a meeting with our experts or see a demo at our booth.
OmniComm Systems is a proud Knowledge Sponsor at SCDM 2019 (Society for Clinical Data Management). Please stop by Booths #402 and 418 to meet our team.
Email firstname.lastname@example.org to schedule a meeting with our team.
Email email@example.com to ensure you are on our invitation list!