RegulatoryID
Integrated Global Regulatory Intelligence
Regulations shift constantly across U.S. federal, state and international regulatory requirements. RegulatoryID gives your team a single, expert-maintained resource for every obligation relevant to your business, so your compliance, finance and legal teams can focus on the work instead of tracking down requirements.
Included with MCR, or available as a standalone license.
What It Does
Regulatory Intelligence, Organized for Action
Tracking regulatory requirements across jurisdictions manually is time-consuming, error-prone and increasingly difficult as requirements multiply. RegulatoryID replaces that burden with a searchable, filterable compendium maintained by MedPro’s compliance professionals, giving your team a single, authoritative source for every requirement relevant to your business.
Searchable Global Compendium
Search and filter regulatory requirements across 50+ countries by manufacturer type, topic, region, jurisdiction and regulatory status in seconds. Find what you need without manually tracking down content from industry, legal and government sources.
Visual Summaries and Detailed Navigators
Access requirements at the level of detail your team needs. Visual Summaries provide high-level overviews of requirements across all jurisdictions in scope. Detailed Compliance Navigators consolidate requirements from laws, regulations and guidance documents in one location, with links to authoritative sources and side-by-side version comparison when requirements are updated.
Proactive Regulatory Alerts
Receive timely alerts and email reminders when requirements change, deadlines approach or new obligations are enacted in the markets you report in. Your team is notified before changes affect your next reporting cycle.
Broad Coverage Across U.S. and Global Requirements
RegulatoryID covers U.S. aggregate spend transparency, gift bans and limitations, field rep registration and licensure, compliance program requirements and international national laws, industry codes, association-based requirements (including European Federation of Pharmaceutical Industries and Associations (EFPIA) and MedTech Europe) and disclosure templates.
The MedPro Difference
What Sets RegulatoryID Apart
Researched and Maintained by Our Global Regulatory Team
Every entry in RegulatoryID is researched, written and verified by MedPro’s global compliance professionals. It is a curated, expert-maintained resource your team can rely on for accurate, current regulatory intelligence, written in plain language that compliance, finance and legal teams can act on directly.
Structured for How Compliance Teams Work
RegulatoryID is designed for the workflows of compliance professionals. Visual Summaries make it easy to get a quick read across multiple jurisdictions. Navigators go deep when precision matters. Filters remove the noise so your team sees only what is relevant to their program, without parsing full legal texts or tracking down guidance documents from multiple sources.
Connected to the Full MCR Platform
As part of MCR, RegulatoryID connects your regulatory intelligence directly to the reporting workflows it informs. Changes flagged in the compendium flow through to the obligations they affect, keeping your team ahead of requirements without manual reconciliation across separate tools.
Version Tracking Built In
When requirements change, RegulatoryID retains version history and provides side-by-side comparison with highlighted changes, so your team can review exactly what changed and when, without re-reading full regulatory texts.
Licensing Options
Included with MCR or Available Standalone
RegulatoryID is included for all MCR customers and is also available as a standalone license for organizations that need regulatory intelligence without the full MCR ecosystem. Contact a MedPro representative to discuss standalone licensing options.
The Platform
How It Fits
RegulatoryID is the regulatory intelligence layer within the MCR platform. It supports U.S. and Global Reporting by keeping your team current on the requirements that govern each reporting obligation, and it operates as a standalone resource for organizations that need regulatory intelligence outside of a full reporting workflow.
Who It’s For
For Teams That Need to Know What the Rules Are
FAQ
Frequently Asked Questions
RegulatoryID Updates
The Latest From RegulatoryID
Each month RegulatoryID publishes a short update on the disclosure deadlines and regulatory changes compliance teams need to plan for. Read the latest issues below, or sign up from any issue to get the next one by email. The updates are one part of RegulatoryID; the full compendium, navigators and alerts live inside the platform.
Provider Verification Beyond Compounding Pharmacy Onboarding
Where Prescriber Verification Fits in the Specialty Pharmacy Workflow
7 Workflow Gaps That Slow Down Life Sciences Compliance Teams
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See RegulatoryID 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 RegulatoryID, tailored to the markets and obligations relevant to your team.
Included with MCR, or available as a standalone license.
