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
Type in the name of the feature or in your own words tell us what you need
Supported
Study eSafe supports regulatory document management, including storage, versioning, and routing.
Study eSafe alternatives
StudyTeam
Better fit for enterprise businesses. Higher ratings. Faster website traffic growth. More focused on overall clinical trial management. StudyTeam alternative. StudyTeam competitor.
Better for creating scientific visuals. Geared towards researchers and academics, especially in life sciences. Has a faster website traffic and employee growth. BioRender is a Study eSafe competitor and alternative.
Better for enterprise networking and offers advanced security features. Not designed for research document management. A Cisco Routers alternative for regulatory document management.
Better for organizations needing electronic signatures for general business documents, rather than specifically for clinical research regulatory documents. More suitable for a broader range of industries.
Better suited for enterprise-level research sites. Has broader industry applicability including Healthcare and Education. Is growing faster and offers more features like remote monitoring and e-signatures. Users love its ease of use and customizability, but dislike the login timeout and document navigation. Generally receives positive feedback regarding pricing. Study eSafe alternative; Study eSafe competitor.
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?
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?
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?
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?
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?
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.