Navigate Life Sciences Transparency Requirements with Ease

Stay informed on current and evolving transparency regulations impacting the Life Sciences industry with RegulatoryID. Researched, written, and verified by MedPro’s in-house team of pharmaceutical and medical device compliance professionals and attorneys, RegulatoryID offers a centralized, easy-to-use resource library of Federal, State, and International requirements, including:

  • Transparency Reporting
  • Gift bans and limitations
  • Field representative registration and licensure (US Only)
  • Compliance program requirements (US Only)

Track News and Reporting Deadlines with Proactive Notifications

RegulatoryID offers proactive updates on transparency related industry news, evolving requirements, and deadline reminders via email alerts. These updates are searchable and appear within the InfoCenter when logging into RegulatoryID.

Quick Search, Filter, and Highlight Relevant Information for your Business

All information is fully searchable and can be easily shared within your organization using the download and email functionality embedded within the platform. Content can also be quickly filtered to your organization's specific needs or use cases:

  • Manufacturer Type: Narrow down the requirements to those impacting your business, whether your organization is a drug or device manufacturer
  • Topic: Look specifically at the use case of interest, be it transparency reporting, gift bans, field representative registration, or compliance program requirements
  • Region: content into US-based (Federal, State, Local) or International requirements
  • Status: Focus on currently enacted obligations, pending legislation, or archived requirements

Reference Content in High-Level Summaries or Detailed Guides

RegulatoryID returns content in two levels of detail:

  • Visual Summaries provide a quick reference guide of 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 head-to-head with highlighted changes for quick review

Streamline Global Transparency Coverage

With comprehensive information for more than 50 countries across five continents, including industry association-based requirements such as EFPIA and MedTech Europe, RegulatoryID synthesizes all global disclosure requirements into an easy-to-navigate compendium, breaking down law and industry association code-based requirements.

Integrate Leading Reporting Software & Support

RegulatoryID is included for all MedPro ComplianceReportingID customers, or can be licensed as a standalone solution

MedPro’s Compliance Advisory Services engages with manufacturers at all stages of their lifecycle to build out or enhance all elements of effective compliance programs, including robust transparency programs.

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“RegulatoryID is very user-friendly and the content is great!"

- VP Compliance, MedPro Customer

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Learn More About RegulatoryID

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