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Global Transparency Reporting: Simplified

International reporting obligations vary by country. See how MedPro Systems tracks them and helps you report accurately everywhere you operate.


MedPro Systems
Published
Updated
Jurisdiction

Country by country

Rules Set By

Local laws, industry codes and enforcement guidelines

Recipients

Often expanded, including patient organizations

Timelines

Vary by country and activity

Global Reporting Requirements Vary by Country

Transparency reporting has become a critical and increasingly complex requirement for Life Sciences companies operating across the globe. Unlike U.S. transparency regulations, international reporting 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 can be triggered by activity beyond sales, such as clinical studies conducted in a country.

This complexity can quickly overwhelm internal teams, which is why MedPro provides the trusted data and compliance solutions needed to ensure accurate, timely reporting everywhere you operate.

MedPro’s Approach to Regulatory Research

Our experts continuously track global transparency regulations, industry codes, emerging laws and best practices. This research is consolidated into RegulatoryID, MedPro’s comprehensive centralized library of international transparency reporting requirements.

With RegulatoryID, you’ll find the guidance you need in one authoritative source, removing the burden of manual research and reducing the risk of missed or outdated requirements.

Globe linked to regulation documents

Holistic U.S. federal and international reporting guidance

Loi Bertrand disclosures due alert with email notification

Proactive updates on evolving regulations and approaching deadlines

Filters for topic, region, manufacturer type and status

Quickly search or filter regulations by topic, region, status and more

The Netherlands Transparency Navigator with linked source

All authoritative sources and related reporting platforms linked for quick access

Regulation version history with enacted and archived versions

Track and compare a regulation’s version history to highlight impactful changes

United Kingdom gift bans resource with send and download options

Direct download and email of resources for distribution to key stakeholders


What Each Navigator Covers

  • Reportable recipients
  • Reportable Transfers of Value (ToVs)
  • Guidance on VAT, language, currency, preemption and cross-border activity
  • Required reporting elements
  • Links to industry codes, guidance documents, templates and forms
Sample Transparency Navigator for the Netherlands

How MedPro Systems Can Help

MedPro brings clarity to complex global requirements. Through MedPro Compliance Reporting ID®, our centralized single sign-on platform, you gain one place to manage global transparency obligations, backed by a team of regulatory experts.

FAQ

Frequently Asked Questions

International obligations vary by country and come from a mix of local laws, industry codes and enforcement guidelines. Many cover a wider set of recipients, such as patient organizations, on their own timelines.

Depending on the country, reportable recipients, reportable transfers of value and required reporting elements, with guidance on VAT, language, currency, preemption and cross-border activity.

Obligations can come from activity beyond sales, such as clinical studies conducted in a country.

Where permitted, yes.

Global Transparency Guide

Navigating Global Transparency Compliance

Download MedPro’s comprehensive guide to global transparency compliance. Learn how leading Life Sciences organizations achieve end-to-end coverage across U.S. and international disclosure obligations in a single platform.

Keep reading

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