Learn about your organization’s current obligations and stay up-to-date with evolving legislative changes impacting the Life Sciences industry with RegulatoryID™. Researched, written, and edited 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 Local requirements covering:
RegulatoryID offers proactive updates on transparency related industry news, evolving requirements, and deadline reminders via email alerts. This information can be easily shared within your organization using the download and email functionality embedded within the platform.
RegulatoryID is included at no extra cost to all MedPro ComplianceReportingID™ customers or can be licensed as a standalone solution.
All information is fully searchable, can be filtered by pharmaceutical or medical device manufacturer specific requirements, and returned in two levels of detail:
MedPro’s Compliance Advisory Services team can also build out or enhance all elements of effective compliance programs, including robust transparency programs.Request a Demo
years providing exceptional value to the industry
Life Sciences organizations trust MedPro
leading Pharma businesses trust MedPro
records in MedProID, the industry’s leading database
“RegulatoryID is very user-friendly and the content is great!"
- VP Compliance, MedPro Customer
Contact us today to get a complete overview of the RegulatoryID module.