MPDmanager - Your IDMP Software and Master Data Management Solution.
Achieve a unified source of truth for your IDMP, XEVMPD, and other medicinal product data.
Are you able to stay abreast of regulatory demands?
As the number of registrations grows, maintaining compliance with regulations becomes progressively challenging.
Ensuring compliance with XEVMPD and IDMP regulations should be effortless.
Data accuracy:
Validate your data comprehensively with business, technical, and internal checks.Centralized repository:
Effortlessly oversee all medicinal product information within a unified platform.Regulatory adherence:
Effectively manage all IDMP, XEVMPD, and CORE data pertinent to your regulated products.Agency connectivity:
Utilize the EMA SPOR database to access agency reports linked to relevant product information.
We Provide Best Digital Services to Grow your Business
- EASILY MANAGE ALL YOUR PRODUCT INFORMATION IN A SINGLE PLATFORM
- ASSURE DATA RELIABILITY AND QUALITY VIA BUILT-IN VALIDATION
- EFFICIENTLY MAINTAIN XEVMPD AND IDMP DATA
Every life sciences company is concerned that incorrect or outdated medicinal product information may put the health of patients at risk and cause product recalls. MPDmanager powered by CARA provides a way to effortlessly manage worldwide product registration data, enabling you to minimize compliance risks and trust that the data you rely on is accurate and up-to-date.
A single solution for thousands of registrations. Maintain your data the easy way. Connect directly to regulatory agencies. Simplifying the move from XEVMPD to IDMP. Simplify Global Regulatory Compliance.
Discover our company's essence. With a blend of experience and innovation, we're committed to delivering top-tier solutions. Unveil our journey, values, and expertise, and join us in shaping excellence.
