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Global Disclosure

One Platform for Every Obligation

Global transparency programs shouldn’t require disconnected tools, fragmented workflows and multiple vendor relationships. MCR brings every international disclosure obligation into a single, centralized platform that scales with your business, so your team can manage every market with consistency and confidence.


Optimize your global transparency reporting in as little as 2 months.

MCRInternational JSJane Smith
InfoCenter Spend Reporting Settings
DISCLOSED SPEND
$35.2M
COUNTRIES
50+
RECIPIENTS
19,953
MARKETLANGUAGESTATUS
France Français Translating… Submission-ready
Germany Deutsch Submitted
Japan 日本語 In Review
Brazil Português Preparing

What It Does

Every Market, Managed from One Platform

Global transparency obligations have grown to span more than 50 countries, each with its own disclosure requirements, industry association frameworks and enforcement environments. MCR was built to accommodate that complexity, adapting to the unique requirements of every market you operate in while keeping your entire global program visible and manageable from a single platform.

Centralized Multi-Country Reporting

Manage disclosure obligations across 50+ countries in a single platform, with a single view of spend across countries and reporting centers. MCR scales with you as you enter new markets without requiring platform changes or additional vendor relationships.

Built-In Approval Workflows

MCR’s approval workflow hierarchy is configurable by jurisdiction and user permissions, giving your compliance and finance teams the controls they need to manage multi-country review and sign-off processes directly within the platform.

English to Reporting Country Language Translation

MCR translates disclosure content into the language required for submission in each reporting country, removing a manual step from the international reporting process and reducing the risk of translation errors in submitted reports.

On-Demand International Report Generation

Generate fully prepared international disclosure reports on demand in the formats required for submission in each jurisdiction, including both submission-ready and review-ready outputs.

The MedPro Difference

Why Life Sciences Organizations Trust MCR for Global Reporting

One Platform, One Team, Every Market

MCR provides a single centralized platform for your full global reporting program, supported by one consistent in-house team who knows your business and the requirements in every market you report in. Your reporting stays connected and visible across every market without the complexity of managing regional vendors and fragmented systems.

A Platform Built for Complexity

MCR supports in-app reporting, single sign-on and managed file transfers across all markets, with embedded dashboards powered by Oracle Analytics Cloud. Machine-learning auto-mapping of configuration data reduces manual setup time when entering new markets or adapting to regulatory changes.

Ahead of Every Change

MedPro’s global regulatory team does not wait for changes to reach your reporting before acting. When a new requirement is enacted or an existing one is revised, your team is notified and the platform is updated before your next reporting cycle.

Scalable from Startup to Global Enterprise

Whether you are reporting in one country or fifty, MCR scales with you without disruption. The same platform that supports an emerging company’s first international obligation supports 9 of the top 10 global pharmaceutical manufacturers managing complex multi-country programs.

Integrations

Capture the Right Data at the Point of Spend

Transparency reporting is only as accurate as the data captured at the point of expense. MedProID® integrates directly within your Travel and Expense platform, giving field representatives access to authoritative HCP data when recording expenses. Spend data then exports automatically to MCR on a daily, weekly or monthly basis, arriving matched and ready for reporting without manual data collection.

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The Platform

How It Fits

Global Reporting is the international disclosure layer within the MCR platform. It works alongside U.S. Reporting for organizations managing both domestic and international obligations and connects with RegulatoryID for in-depth regulatory intelligence on international requirements. All modules share a single platform, a single sign-on and one consistent in-house team.



50+
Countries Covered
99%
Customer Retention Rate
95%
Of Data Review Requests Resolved Within 1 Business Day

Recent Testimonials

What Our Customers Say

Our international data is laid out cleanly in the tool. It’s very different than what we’ve seen elsewhere.

I want to extend our appreciation to the MedPro team. Your collaboration on the project, and the hours spent reviewing our company’s portfolio, projects, and data analysis has proven invaluable. Your expertise and insights have streamlined our processes and empowered us to establish an effective reporting framework. Thank you for your dedication and commitment to upholding our standards of excellence.

MedPro’s large customer base could create great benchmarking for clients less experienced with State Drug Price Transparency.

Read Customer Stories

FAQ

Frequently Asked Questions

MCR supports transparency reporting obligations across 50+ countries, covering national laws, industry association-based requirements (including European Federation of Pharmaceutical Industries and Associations (EFPIA) and MedTech Europe) and regional codes. RegulatoryID, included with MCR, provides a searchable compendium of requirements for each country and jurisdiction.

MedPro’s global regulatory team monitors international requirements on an ongoing basis and issues proactive alerts when requirements change in the markets you report in. Updates are reflected in the platform and communicated directly to your team before they affect your next reporting cycle. All MCR customers also receive quarterly compliance reviews with their dedicated support team.

Yes. MCR includes a built-in approval workflow hierarchy that is configurable by jurisdiction and user permissions, allowing your compliance and finance teams to manage multi-country review and sign-off processes within the platform.

MCR translates disclosure content into the language required for submission in each reporting country, removing a manual translation step and reducing the risk of errors in submitted reports.

Yes. MCR provides end-to-end coverage for both U.S. and international transparency obligations in a single centralized platform, with one consistent in-house team supporting your team across every jurisdiction you operate in. U.S. and international reporting are managed within the same environment with a single sign-on and cross-application reporting visibility.

Global transparency disclosure requirements are the laws, industry codes and regulatory frameworks outside the United States that require Life Sciences manufacturers to report financial interactions with healthcare professionals and healthcare organizations in the countries where they operate. These vary significantly by jurisdiction, shaped by national legislation, industry association codes such as the European Federation of Pharmaceutical Industries and Associations (EFPIA) and MedTech Europe, and regional standards, each with different reportable recipient categories, transfer of value classifications, language requirements and submission timelines. MCR supports global transparency reporting across 50+ countries in a single platform, with built-in language translation, multi-country approval workflows and proactive regulatory change monitoring through RegulatoryID.

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See Global Reporting in Action

Submit your information to connect with a MedPro representative. We’ll reach out to schedule a 30-minute strategy session and live demonstration of MCR’s Global Reporting, configured to your compliance needs.

Optimize your global transparency reporting in as little as 2 months.