RegDesk vs. AmpleLogic Regulatory Information Management System

RegDesk stands out as the leading RIMS platform enhanced by AI, tailored specifically for Medical Device, Pharmaceutical, and IVD companies. • Our unique Regulatory Intelligence encompasses data from over 120 countries, all presented in a uniform format, and includes timely alerts regarding regulatory updates. • With our AI-driven Application Builder, regulatory affairs teams can efficiently create and submit global applications in a fraction of the usual time. • The Change Assessment feature enables RA teams to evaluate the implications of changes on current products and determine the necessary actions. • Our Distributor Collaboration tool facilitates smooth workflows for communication and document sharing with external partners. • The Standards Management function simplifies the process for RA teams to locate and oversee both international and country-specific standards. • Additionally, our Tracking & Reporting capability empowers teams to monitor regulatory initiatives worldwide, receive notifications for renewals, and quickly compile reports on key performance indicators. To learn more about our offerings, please explore our website.

The AmpleLogic Regulatory Information Tracker, created using a LOW CODE AND NO CODE (LCNC) PLATFORM, features two main elements: the ANDA and DMF Tracker. This software serves as a vital tool for managing pharmaceutical regulatory information, aimed at improving data accuracy, boosting operational efficiency, reducing mistakes, and promoting seamless communication across different departments. Implementing this solution enables organizations to foster enhanced collaboration while ensuring adherence to regulatory requirements. Ultimately, it supports better decision-making processes and reinforces compliance efforts within the industry.