Clinical Trial Templates and Electronic Source for Clinical Trial

Expertly Building Electronic Source for Clinical Trial & Clinical Trial Templates

eSource (document) refers to an electronic source for a clinical trial that contains all of the data required by the study protocol for all visits. The goal of our data operations and quality assurance teams is to create an eSource that is a duplicate of the sponsor’s electronic data capturing (EDC) systems in compliance with the research protocol.

At Minerva Research Solutions, our data operations and quality assurance teams work closely with CRCs to ensure clean and efficient data entry into EDCs, streamlined eSource building, and adherence to protocol and eCRF guidelines. Through our use of the CTMS, we develop clinical trial templates that follow the study protocol’s Schedule of Activities (SOA) and eSource which are identical duplicates of the eCRF.

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Reducing Deviations by developing Clinical Trial Templates & eSource

Minerva Research Solutions’ highly competent data operations and quality assurance teams put in a lot of effort to produce an accurate eSource that is identical to the eCRF guidelines, adhering to study protocols. Our goal is to reduce protocol deviations, data costs and ensure your clinical trial receives a clean bill during FDA inspections.

We aim to help research sites eliminate paper, improve the quality of data and increase efficiency through our electronic source for clinical trials and clinical trial template-building processes in CTMS. We help your sites save time on visits through accurate scheduling of visits and protocol-specified procedures through our template building that helps sites capture data. Our goal is to ensure that sites always remain monitor-ready. Our quality assurance team works hard to establish that your study has completed source data.

What Makes Us Unique

Seamlessly Managing Your Clinical Research Site and Patient Data

Our solutions are built for research sites. We aim to streamline your site’s operations, help you collaborate in real-time, and ensure that you can access clinical trial data anywhere by going completely paperless.

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Efficient Entry of Scientific Data

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Streamlined Clinical Trial Templates & eSource Building

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Optimized Data Management through Electronic Source for Clinical Trial

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Have questions?

How long does it take to resolve queries in clinical trial templates & electronic source for clinical trial?

Minerva’s data operations and quality assurance teams ensure that all queries generated by the eSource or in the EDC are resolved within 24 hours.

How does the Minerva Research Solutions quality assurance and data operations teams develop eSource?

eSource building is done once we receive the eCRF guidelines after the SIV is completed, keeping in mind the protocol guidelines. This is then reviewed by the respective CRC.

What software do you use to develop eSource and clinical trial templates as a part of data operations?

The software used for building templates and electronic source for clinical trials is RealTime-CTMS.

Who handles the eSource building?

In Minerva Research Solutions operations, the data operation and the quality assurance teams work on developing the eSource which is then further reviewed by the Clinical Research Coordinator (CRC). The quality assurance team will ensure that the eSource is up-to-date as per any amendments in the study protocol that comes through.

Expertise that leads to Efficient Clinical Trial Template & Streamlined Development of Electronic Source for Clinical Trial

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Templates & eSource (Electronic Source) for Clinical Trial