Freya Reviews & Product Details

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.

Essenvia is a MedTech RIM Platform to manage regulatory workflows across the total product lifecycle, accelerate global market access, and generate exponential business value. The Platform makes the lives of MedTech Regulatory Teams easier by supporting Global Registrations, Submissions, Change Assessment, and Regulatory Intelligence.

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