Smart Regulatory Review process
Faster access to Global regulations
Global regulatory status on a click
A SmartTech platform for efficient RA process
VITALIC® - the RIMS Software by DDReg for Regulatory Submission Management and Compliance helps pharma organizations stay updated on the complex web of global regulatory requirements while also helping them develop submission packages and track submitted applications on global basis. It captures global regulations and templates for ready access for regulatory teams across the globe within pharma organizations. Lifecycle tracking tool of VITALIC® helps the decision makers, departmental heads , business heads and the management to track and monitor the global regulatory status of filings and provides ‘at a glance’ visibility of the global status.
Key Vitalic® Capabilities
VITALIC® is a cutting-edge platform that combines regulatory project management with valuable regulatory insights to make registering and renewing products a breeze. The platform uses proprietary technology to provide a web-based, easy-to-navigate user interface that makes it simple for users to manage projects, monitor progress, and prepare submissions. The built-in templates help users author documents that meet country-specific requirements. The platform's efficacious tools keep track of all project-related information in one place, including region-specific timelines, approval processes, waivers, patents, and fee structures. The platform also provides alerts and notifications to keep users constantly updated so they never miss a deadline or important update.
VITALIC® is equipped with the latest regulatory intelligence, data, documentation, and insights from over 130+ countries, making it easier to anticipate rapidly changing global regulatory developments and manage the product lifecycle. Whether you're a regulatory professional or a business owner, VITALIC® is the ultimate solution for managing your Regulatory Process Management needs and delivering the data you need when you need it.
VITALIC® is the ultimate solution for Regulatory Process Management. With its compliant procedures, tools, and controls, the platform ensures compliance with regulatory policies, requirements, and standards, regardless of the region. VITALIC® streamlines access to relevant information optimizes project planning and tracking, and minimizes replication of effort, making it the perfect solution for managing the complexity and variability of the regulatory process. Whether dealing with multiple products or navigating different regulatory requirements, VITALIC® is the ideal platform for streamlining and simplifying your Regulatory Process Management needs.
Regulatory Information Management (RIM) Software
An effective Regulatory Submissions Management Solution combines regulatory document managements, global regulatory intelligence on real time basis with innovative technologies that tackle challenges pertaining to ever-changing regulations, submission delays and more. It makes product application with use of efficient document management, data management and process management. Such high quality submission packages, when processed by regulatory agency/competent authorities, lead to minimal or no queries thereby preventing rejections.
Technology to propel your Regulatory efficiencies to next level
VITALIC® helps pharmaceutical organizations to better manage their regulatory information to gain rapid market access while ensuring regulatory compliance through efficient information management systems