Resource Library
Your one-stop-shop for regulatory, clinical, and quality insights, from whitepapers to webinars to how to guides.
Webinar: Compliant Trial Master File Management & Migration in 2024
For many small and mid-size Clinical teams, the TMF struggle is real. Maybe you’re using your CRO’s eTMF for now - but what happens after study completion? Or maybe you’re trying to save...
Webinar: Collaborating with your CRO for Study Compliance
Today's clinical trials are partnerships, between Sponsors, CROs, and other vendors. These collaborations enable small organizations to do more, but it also presents challenges. In this...
Webinar: IT Best Practices for TMF Transfers from CROs
In this session, Kivo CEO Toban Zolman and SVP of Clinical Marion Mays outline the best information technology practices for accepting, managing, and storing trial master files,...
Webinar: Best Practices for End of Study TMF Transfer
Do you have a plan for receiving your TMF from your CRO soon? Have you mapped out your strategy and how you will ensure you are maintaining the chain of custody for what is one of...
Webinar: CTIS Technical and Process Implications for Sponsors of EU Clinical Trials
In this webinar, Kivo CEO Toban Zolman and SVP of Clinical, Marion Mays outline the implications of the upcoming requirement to leverage the CTIS portland for all clinical trials taking...
Webinar: Compliance Meets Collaboration - TMF Inspection Readiness
In this webinar, Kivo CEO Toban Zolman and SVP of Clinical Marian Mays discuss the differences between an in-person inspection and the more recent virtual or hybrid inspections....
Webinar: Managing IND Submissions Using Lean Principles
In this webinar, Kivo CEO Toban Zolman and Director of Regulatory Theresa Pinnell discuss how to apply Lean methodologies to the regulatory submission process, focusing on an IND submission...