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Your Clinical Trial Deserves TLC From PRC

eTMF & Document Management

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We offer eTMF solutions that utilize cutting-edge technologies and practices to manage the essential document control of your trials. Whether you need to manage Investigator Site Files (ISF) or the larger Trial Master File that includes Investigational New Drug (IND) application and required documents, we have the expertise to handle it all. You can trust us to manage everything efficiently and effectively.

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Certified User Team

PRC Clinical’s team is the ultimate choice for constructing and managing your TMF with the utmost expertise and precision. Their certifications and experience make them the most qualified team to ensure the accuracy and quality of your study documents and electronic files. You can confidently trust in our proficiency to deliver exceptional results.

Audit Ready Documents

Our rigorous quality control process involves subjecting each document to multiple reviews by different qualified individuals. This meticulous approach ensures that the quality of each document is thoroughly examined for accuracy and completeness. As a result, our clients are assured their electronic files and documents are always audit-ready and inspection-ready.

Automated Technology

The utilization of Artificial Intelligence (AI/bots) and automation in the electronic Trial Master File (eTMF) software greatly enhances the consistency and qualify standards of clinical trial documents. By integrating these cutting-edge technologies into our highly standardized processes and electronic TMF software, the TMF and associated (auditable) metadata can attain even higher levels of efficiency and accuracy.

Does Your Trial Need TLC From PRC?

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