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IT Best Practices for Receiving eTMFs from CROs

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 your most valuable assets? The TMF is the story of your clinical study and needs to be handled appropriately. Key areas covered:

  • Planning for the handover of the study TMF
  • Key considerations when migrating or transferring a study
  • What all should be included in the export for compliance
  • Regulations to support Data Integrity

Join Kivo's CEO, Toban Zolman and Clinical Expert, Marion Mays, for best practices on end of study TMF transfer.

Date: Friday August 25th, 2023

Time: 10am PST (1pm EST)

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About the Presenters

Marion Mays brings extensive experience in Inspection Readiness and supports clients in their efforts to become fully inspection-prepared. Marion is a dynamic, inspirational leader in the Life Sciences space with over 30 years of experience. Offering a unique combination of both strategic and operational abilities she also has in-depth experience with quality and compliance processes in the pharmaceutical industry with focus on supporting organizations through GCP regulatory inspections with FDA, MHRA, EMA, and PMDA. Her experience working for sponsors, CROs, software vendors and directly helping sponsors manage inspections make Marion uniquely positioned to offer valuable insights into this process.

 

Toban Zolman has extensive experience solving complex business challenges using software. Toban was an early employee at Regulatory software pioneer ISI, helping shape the transition to electronic submissions. He has worked with dozens of the largest global pharmaceutical companies to define business processes around clinical and regulatory processes. Toban is CEO of Kivo, a software provider focused on streamlining the drug development process for emerging life science companies.

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eTMF Reference Model

Kivo organizes documents using the familiar eTMF reference model making it fast to learn and easy to train.

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Integrated Digital Signatures

Customizable Collaboration, Review, and Approval workflows with Part-11 Compliant Digital Signatures.

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Economical, straightforward pricing

Comprehensive pricing gives you access to every Kivo feature, and ongoing releases.

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Smart Document Placeholders

Reuse content, assign documents to users, and always have visibility into when content will be completed.

Clinical Document Management That Works Like You Do.

 

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