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  6. Clinical Trial Document Management System - Case Study at Riverfield Inc.

Clinical Trial Document Management System - Case Study at Riverfield Inc.

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last updated:Jan 21, 2025

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Achieve efficiency and accuracy in operations with Agatha SOP and Agatha QMS!

We would like to introduce a case study on the implementation of "SOP Management and Training Records" and "Agatha QMS" at Riverfield Inc., which develops medical robots. At the company, operations were conducted using printed documents created in Word and an analog procedure of circulating approvals on paper. After the implementation, they have achieved greater efficiency and accuracy in their operations, and they have reported that urgent approvals can now be obtained in a very short time. [Utilized Operations] ■ Agatha SOP - Review and approval workflow for newly created or revised documents such as various regulations and forms - Implementation of training (Read & Review, confirmation tests) - Viewing of documents such as regulations and forms, and investigation of revision history ■ Agatha QMS - Management of nonconformities, complaint handling, and CAPA management in the QMS for medical devices *For more details, please download the PDF or feel free to contact us.

    Document and Data Management
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Clinical Trial Document Management System - Case Study at Riverfield Inc.

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Clinical Trial Document Management System - Case Study at Riverfield Inc.

Clinical Trial Document Management System - Case Study at Riverfield Inc.

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Our company provides a cloud service for creating, sharing, and storing documents related to clinical trials and clinical research on a project basis for medical institutions, pharmaceutical companies, medical device companies, CROs, SMOs, clinical testing companies, and more. In addition to offering systems specialized for the medical and life sciences industries, we provide comprehensive support from implementation to operation by staff with expertise in the medical field. Please feel free to contact us if you have any inquiries.

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