Manually validating large datasets is slow, labor-intensive, and can't keep up with deadlines, making anomaly detection and reporting overly complex.
Transparency Reporting Solution minimizes manual effort by automating data cleansing, validation, standardization, and organization, ensuring cleaner, compliant, and submission-ready spend reports.
With AI-trained models, compliance teams gain more time, less friction, and greater confidence in the accuracy and integrity of their federal and state level reports.
Aggregate and monitor HCP/HCO spend across federal and state mandates for full transparency.
Automated data validation and CMS/state rule checks minimize errors and ensure report readiness.
Clean, match, and profile data across sources to meet complex reporting requirements with consistency.
Streamlined workflows for monthly/quarterly uploads, report preparation, and recipient validation reduce manual effort.
From data prep to dispute period assistance, the solution supports the full reporting cycle.
Built-in scheduling and deadline tracking help teams meet CMS and state submission timelines with confidence.
Aggregate spend data from all relevant systems and platforms into a single, unified pipeline for reporting.
Establish the foundational logic that governs how data is interpreted and processed throughout the reporting cycle.
Automate scheduled data ingestion and apply rigorous validation checks to ensure data integrity before processing.
Apply AI-trained models to classify, analyze, and clean spend data, surfacing potential issues before submission.
Generate fully compliant, submission-ready reports for both CMS and state-level requirements.
Support compliance teams through the full post-submission lifecycle, from error resolution to analytical reporting.
Compliance Reference
Open Payments — CMS Section 6002
Applicable Pharmaceutical, Medical device manufacturers, and Group Purchase Organizations (GPO).
All payments, gifts and other transfers of value made to U.S. physicians and teaching hospitals including:
Annual reports must be submitted to the Centers for Medicare and Medicaid Services through the online portal at portal.cms.gov
Pharmaceutical Sales Representative Reporting
A list of HCPs who have been provided by a pharmaceutical sales representative:
Data points to be disclosed: Manufacturer name, Representative State ID, Transaction Date, Recipient Name, Professional Designation, NPI, Zip Code, Compensation Amount & Type; and if a sample drug was provided: Drug Name, NDC.
Submit the template file as an attachment via email to: drugdatabase@dhhs.nv.gov
Pharmaceutical Manufacturer Reporting
Payments, reimbursement or other compensation paid to HCPs registered and practicing in Minnesota during the calendar year in which the transfer of value is $100 or more to a particular covered recipient.
Data points: Name of practitioner, Professional designation, Address, Value of payment, Specific reason for payment.
Reports must be filed electronically. Complete the spreadsheet available on the Minnesota Board of Pharmacy website and return it attached to an e-mail at pharmacy.board@state.mn.us or on a CD-ROM.
Pharmaceutical Manufacturers and Labelers
Submit the Excel workbook containing "Company Information," "Gift Expenses," and "Advertising Expenses" worksheets via email to doh.accessrx@dc.gov. Mail signed Company Information worksheet and a $5,000 check payable to "D.C. Treasurer" to: Department of Health, Pharmaceutical Control – AccessRx, 899 N. Capitol Street, NE, Second Floor, Washington, D.C. 20002.
Pharmaceutical Company Representative Reporting
An individual authorized, certified, and licensed under the laws of Oregon to prescribe, dispense or provide pharmaceutical products to patients for treatment, diagnosis, injury, congenital or disease prevention.
Interactions healthcare professionals have with pharmaceutical representatives including video conference, email, telephonic conversation, in-person meetings, or leaving material/drug samples.
No exemptions.
A disclosure log must be submitted via the iReg Portal before April 1st. The reporting spreadsheet is available on the Oregon DFR website.
Pharmaceutical and Medical Device Manufacturers
Manufacturers must register with the Department of Public Health and pay a yearly fee of $2,000. Email the CSV file attachment with subject line "[Year] Disclosure Report" to dph.pharmaceutical.disclosure@state.ma.us
Pharmaceutical Manufacturers
Any pharmaceutical manufacturer that employs individuals to perform the duties of pharmaceutical sales representatives in the U.S.
Payment or other transfer of value, except when the transfer is made indirectly to an APRN via a third party and the applicable manufacturer is unaware of the APRN's identity or meets the exclusion criteria set by CMS Open Payments.
Data points to be disclosed:
Email report to DCP.DrugManufacturers@ct.gov with the subject line "APRN Payment Report." An auto-response will be sent to the submitter's email address as proof of submission.
Any pharmaceutical manufacturer that employs individuals to perform the duties of pharmaceutical sales representatives in the U.S.
Data points to be disclosed:
Email report to DCP.DrugManufacturers@ct.gov with the subject line "CT Sales Rep Report." An auto-response will be sent to the submitter's email address as proof of submission.
Pharmaceutical and Medical Device Manufacturers
Complete and submit the Compliance Officer Form by January 1st of each reporting period with a registration fee of $500. Email completed Excel spreadsheets for both Expenditure and Sample disclosures to ago.disclosures@vermont.gov
Section 6004 of the Affordable Care Act — Drug Sample Reporting
Manufacturers and authorized distributors of applicable drugs must submit the identity and quantity of drug samples requested and distributed, aggregated by:
Data points to be disclosed: Submission year, Business name, Practitioner professional designation, First/middle/last name, Address, Drug trade name and dosage, Package size, Package/quantity requested, Package/quantity received, Signature received.
When a manufacturer and authorized distributor of record (ADR) both have records regarding the same drug sample request or distribution, only one of the two entities should submit the required information to FDA.