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:
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.
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:
RegulatoryID returns content in two levels of detail:
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.
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.Request a Demo
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“RegulatoryID is very user-friendly and the content is great!"
- VP Compliance, MedPro Customer
Contact us today to get a complete demo of the RegulatoryID module.