Top 10 Alternatives to Essenvia Recently Reviewed By G2 Community
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Your all-in-one SOP, document control and training solution. Automate the creation, review, approval and management of Policies, Procedures, Work Instructions, Forms and related content.
MasterControl Inc. produces QMS software solutions which enable regulated companies to get their products to market faster, while reducing overall costs and increasing internal efficiency. MasterControl securely manages a company's critical information throughout the entire product lifecycle.
Research Manager supports researchers and organisations in preparing, executing and administering (clinical) research data. Our expertise is the collection, validation and enrichment of data. With Research Manager, we offer a research platform that allows researchers to have all functionalities and information in one place and to share it with each other. The platform facilitates researchers who want to be prepared for a future where the patient, access to data, and sharing data are key.
Kivo makes simple and affordable document management systems including RIM, eTMF, and QMS. A single license grants access to all our solutions, so you can supercharge cross-functional collaboration without breaking the bank. Fully validated, Part 11 and SOC 2 compliant, Kivo is designed forGxP.
Rimsys is the only Regulatory Information Management (RIM) software built specifically for MedTech manufacturers. Our platform helps medical device and diagnostic companies streamline global regulatory processes by centralizing product registrations, submissions, standards, essential principles, and UDI data for EUDAMED compliance. Trusted by 6 of the top 12 MedTech companies, Rimsys replaces outdated systems with a modern, integrated solution that reduces risk, speeds time-to-market, and transforms regulatory affairs into a strategic revenue driver.
RegDesk is the next generation RIMS software with AI technology built exclusively for medical device and diagnostic companies. It is a one stop solution for regulatory teams.
The Vault RIM Suite provides fully integrated regulatory information management (RIM) capabilities on a single cloud-based platform including submission document management, product registration management, health authority correspondence and commitments, submission archiving, and comes with fully integrated IDMP capabilities.
Validfor is a digital validation lifecycle management platform that modernizes how regulated organizations manage their computerized system validations. Designed for the life sciences, pharmaceutical, and medical device industries, Validfor centralizes all validation activities in one secure and compliant environment. By replacing traditional manual validation with a digital, data-driven approach, Validfor enables teams to plan, execute, and track validation processes with real-time visibility and accuracy. The platform includes built-in templates, electronic approvals, and full traceability to ensure regulatory compliance and consistent documentation quality. Whether you’re managing a single system or an enterprise-wide validation program, Validfor helps your organization stay audit-ready, improve collaboration, and maintain complete data integrity while saving time and reducing compliance risk.
QuickVault unifies product development, regulatory compliance, quality management, and operations in a single, purpose-built cloud solution for MedTech teams.
CRA Manager is a SaaS platform dedicated to Cyber Resilience Act (CRA) compliance management. It helps manufacturers of products with digital elements continuously manage their CRA obligations by connecting products, SBOMs, components and vulnerabilities, risks, remediation actions and compliance evidence in a single platform. CRA Manager also supports technical documentation, including Annex VII, CE marking workflows and vulnerability and incident reporting requirements. Designed for product security, engineering and compliance teams, CRA Manager provides a structured and traceable approach to maintaining CRA compliance throughout the product lifecycle.