Looking for alternatives or competitors to Essenvia? Other important factors to consider when researching alternatives to Essenvia include reliability and ease of use. The best overall Essenvia alternative is MasterControl Quality Management System. Other similar apps like Essenvia are Clinical Research Suite, Rimsys, Kivo, and Veeva Vault RIM. Essenvia alternatives can be found in Regulatory Information Management (RIM) Systems but may also be in Quality Management Systems (QMS) or Clinical Trial Management Systems.
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.
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 Trusted by 6 of the top 12 MedTech companies, Rimsys replaces outdated systems with a modern, integrated solution that reduces risk, speeds time-to-market, and transforms regulatory affairs into a strategic revenue driver.
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.
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.
RIMS (Regulatory Information Management System) allows companies to team up, preserve application information data from various locations and enhance the processes of preparing a submission, as well as simplify the publishing and tracking of all regulatory activities that support a product’s complete life cycle.
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.
This is a trusted industry-ready, cloud-based Pharmacovigilance and Safety Database software. It is pre-validated and is quick to implement, providing faster ROI with the added benefit of data migration. What PvEdge offers: 1. Manage Drug, Device, Vaccines & Combinational Products' Core Case Processing with ICSR Gateway Submission 2. Product Inquiry (MICC Tool) 3. Literature Surveillance 4. Triage Management 5. Specialised for Human & Veterinary Vigilance 6. Safety Data Exchange Agreement System (SDEAs) 7. Pharmacovigilance Quality Management 8. eCTD Publishing - PADER/ PSUR
Freya, Your AI First Regulatory Wiz, is a context-trained Regulatory AI powered chatbot, that allows you to harness the power of regulatory intelligence data with exceptional accuracy and ease. Freya allows you to ask questions and provides verified, referenceable, and authenticated Regulatory information at your fingertips.