Master Global Transparency with MedPro’s End-to-End Reporting Solution

Was your last reporting season hindered by regional data silos or compliance gaps? Centralize your data and automate disclosure with MCR, the end-to-end solution built for the evolving complexity of global transparency.

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Optimize your transparency operations in as little as 2 months.

Global transparency reporting can’t be effectively managed through disconnected tools. When disclosure rules shift across borders, jurisdictions or even industry association-based requirements, self-service methods leave organizations exposed to risk. Most organizations currently face one of three critical hurdles:

  • Reporting Burnout: Many teams are currently feeling the strain of a sub-optimal reporting season characterized by poor data quality, slow acquisition, and a lack of integrated compliance support .
  • Global Scaling: Scaling transparency efforts internationally often reveals growing pains, as disconnected regional silos fail to provide a holistic view of global spend.
  • The Regulatory Moving Target: Transparency is not static; a patchwork of shifting laws codes, and requirements makes it nearly impossible to stay compliant without a ‘living’ regulatory compendium.

You need a holistic approach—a single system of record—to manage spend and regulatory tracking across reporting centers to drive informed commercial operations.

One Centralized Platform for Global Confidence

Trusted by 200 + Life Sciences leaders and backed by 16 years of compliance expertise, MedPro provides the maturity and confidence compliance demands.

Enhanced by best-in-class data and service, our end-to-end global transparency platform, MedPro Compliance Reporting ID (MCR), delivers:

Global Transparency Coverage

Streamlined U.S. Federal Open Payments (Sunshine Act), State, Local and International disclosure.

RegulatoryID Intelligence

A centralized global disclosure compendium of 50+ countries and industry association-based requirements.

Expert Oversight

Proactive monitoring and support from industry experts who translate complex legalities into executable data requirements.

Certified Security

SOC 2 (Type I & II) and ISO (9001 & 27001) certified to provide the security and operational maturity required to manage your most sensitive spend data.

A Simplified Journey to Global Reporting

Optimized transparency operations in as little as 2 months with our rapid deployment of our proven solution paired with embedded compliance partnership from a team of industry veterans.

  • Step 1: Planning & Design – Assessment of your spend data sources and jurisdictional requirements with a dedicated project lead, technical specialists and our global regulatory experts.
  • Step 2: Setup & Customization – Translating regulatory complexities into your system’s configuration requirements and compliance data mappings.
  • Step 3: Approval & Go Live – Full user training, validation and access to centralized global disclosure platform for streamlined reporting.
Disclosure reports generated in the most recent reporting cycle.
Customer records updated in the most recent reporting cycle
of data review requests resolved within 1 business day

The MedPro Standard

Trusted By Leaders Across Life Sciences Industry for:

Authoritative Data

Sourced from verified state, federal and industry sources. 

Seamless Integration

Connects directly to your CRM, MDM and T&E Platforms. 

Trusted Partner

Serving both global enterprises and pre-commercial startups with premier customer support

Proven Results

99% customer retention rate for active Life Sciences organizations.

DRIVEN BY DATA

MedProID is the industry’s most accurate, comprehensive and trusted source of HCP and HCO identifying data, accessible in real-time through a centralized platform that integrates directly with your internal systems.

  • 33 million HCP and HCO Records
  • 25+ Years of Historical Licensing Information
  • 800+ Active Life Sciences Customers

Powered By Service

Collaborate with and rely on our tenured, friendly and knowledgeable team. We don’t just know the data, we know how it can help the operational effectiveness of your business. With over 25 years of experience, you will be supported by our proactive team and personalized service from day one.

  • • “The MedPro team made our implementation seamless. Their swift responses to all our questions speed up the process. Incredible support and always available to help!”
  • “Our MedPro team knows us and is responsive. It never feels like a distant, non-personal service.”
  • “In addition to having excellent customer service, MedPro actively listens and offers solutions to address our concerns. Collaborating with the MedPro team is a fantastic experience.”
  • “I’ve worked with Medpro most of my career and I can honestly say, they have been one of my favorite partners to work with.”

Transparency Reporting FAQ

MedPro’s end-to-end global platform equips you for the growing complexity of transparency obligations. We deliver unmatched reporting technology through a compliance lens. MCR offers a centralized, flexible solution that simplifies the entire disclosure process—with the scalability to meet the needs of both industry leaders and emerging startups.

Unlike U.S. transparency regulations, global disclosure obligations vary significantly by country and are shaped by a patchwork of local laws, industry codes and enforcement guidelines.
 
Depending on the jurisdiction, companies may be required to report certain interactions and/or transfers of value, often to an expanded set of recipients, such as patient organizations, on timelines that vary in frequency and aren’t always tied to commercial activity (e.g., clinical studies conducted in a country).

Yes! Federal U.S. Open Payments reporting is fully supported as well as Federal Drug Samples, State and Local Aggregate Spend. The system supports integrated analytics and automated report generation to streamline compliance.

RegulatoryID delivers structured, searchable access to the full scope of transparency and compliance obligations. Content can be viewed in summary or detail to best fit the needs of your search

  • Visual Summaries: Quickly reference high-level requirements across all jurisdictions in scope per topic.
  • Detailed Compilations (Navigators) outline requirements from disparate laws, regulations and guidance documents in one convenient location, with links to authoritative sources for each topic and jurisdiction. As Navigators are updated, versions can be compared side by side with highlighted changes for quick review

MCR customers can rely on a dedicated project lead, technical experts and the entirety of our global regulatory team throughout the life of the contract. We are highly responsive and proactively monitor the ever-evolving international landscape to help you reduce risk and meet every requirement and obligation.

DEMO THE DIFFERENCE

Submit your information to connect with a MedPro representative. We’ll reach out to schedule a 30-minute strategy session and live demonstration of our configurable MCR solution tailored to your unique global transparency needs.

Optimize your transparency operations in as little as 2 months. Request your session today.

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