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Study eSafe

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Company health

Employee growth
7% decrease in the last year
Web traffic
10% increase in the last quarter

Ratings

G2
5.0/5
(7)
Glassdoor
4.4/5
(13)

Study eSafe description

Study eSafe is a free platform designed for clinical research sites to manage their regulatory and source documents electronically. It helps sites maintain compliance with regulations (21 CFR Part 11) while streamlining document management tasks. The platform offers features like electronic signatures, document version control, expiration tracking, and customizable workflows, enabling efficient collaboration and reducing administrative burdens for research teams.


Who is Study eSafe best for

Study eSafe is a free platform ideal for clinical research sites needing a streamlined solution for managing regulatory and source documents electronically. It simplifies compliance with 21 CFR Part 11 through features like electronic signatures and version control. This eliminates administrative burdens, enabling efficient collaboration.

  • Best fit for small to medium-sized clinical research sites.

  • Specifically designed for the Healthcare industry.


Study eSafe features

Supported

Study eSafe supports regulatory document management, including storage, versioning, and routing.


Study eSafe alternatives

  • Logo of Advarra eReg
    Advarra eReg
    Streamlines research regulatory documents for faster study startup.
    Read more
  • Logo of RealTime-CTMS
    RealTime-CTMS
    Streamlines clinical trials, boosting efficiency and profits.
    Read more
  • Logo of Kivo
    Kivo
    Streamlined document management for life science regulatory compliance.
    Read more
  • Logo of Veeva Vault QualityDocs
    Veeva Vault QualityDocs
    Manage regulated documents efficiently, compliantly, and collaboratively.
    Read more
  • Logo of Agatha Clinical eTMF
    Agatha Clinical eTMF
    Easy clinical trial document management for compliance and collaboration.
    Read more
  • Logo of Octalsoft CTMS
    Octalsoft CTMS
    Streamlines clinical trials, boosting efficiency and compliance.
    Read more

Study eSafe FAQ

  • What is Study eSafe and what does Study eSafe do?

    Study eSafe is a free platform for clinical research sites to manage regulatory and source documents electronically. It ensures compliance with 21 CFR Part 11, offering electronic signatures, version control, expiration tracking, and customizable workflows for efficient collaboration and reduced administrative burden.

  • How does Study eSafe integrate with other tools?

    There is no information available about specific integrations for Study eSafe. It's designed as a standalone platform for managing regulatory and source documents within clinical research sites.

  • What the main competitors of Study eSafe?

    Study eSafe's main competitors include StudyTeam, a platform for clinical trial management, and Advarra eReg, another regulatory document management system. Florence eBinders also offers similar e-binder functionalities for research sites.

  • Is Study eSafe legit?

    Study eSafe appears to be a legitimate platform. It offers a free, compliant electronic regulatory binder solution for clinical research sites, managing regulatory and source documents, and streamlining document management tasks. User reviews are limited, but a 4.35 rating on Glassdoor suggests positive user experiences.

  • How much does Study eSafe cost?

    I cannot find pricing information for Study eSafe. Contact the vendor directly to determine product pricing and if Study eSafe is worth it for your needs.

  • Is Study eSafe customer service good?

    Users highlight Study eSafe's outstanding customer service, exceeding expectations for a free product. They appreciate the program's adaptability and compliance features, further enhancing their positive experience.


Reviewed by

MK
Michal Kaczor
CEO at Gralio

Michal has worked at startups for many years and writes about topics relating to software selection and IT management. As a former consultant for Bain, a business advisory company, he also knows how to understand needs of any business and find solutions to its problems.

TT
Tymon Terlikiewicz
CTO at Gralio

Tymon is a seasoned CTO who loves finding the perfect tools for any task. He recently headed up the tech department at Batmaid, a well-known Swiss company, where he managed about 60 software purchases, including CX, HR, Payroll, Marketing automation and various developer tools.