OAR 836-200-0555
Assessments Against Prescription Drug Manufacturers


(1)

Once annually, no later than October 1, all reporting manufacturers will pay an assessment of $400. The director may by order reduce the fees assessed for any specific year.

(2)

Once annually, no later than October 1, reporting manufacturers that have filed one or more reports under OAR 836-200-0515 (Threshold for Reporting Drug Price Increase) to 836-200-0530 (Form and Manner Requirements for Drug Pricing Reporting) between August 1 of the previous year and July 31 of the current year must pay an additional assessment for each report filed.

(3)

For the purposes of subsection (2), the director shall determine the amount of the assessment by subtracting the revenue collected under subsection (1) from the amount of revenue needed to cover the department’s estimated expenses in administering Oregon Laws 2018, chapter 7, section 2 and OAR 836-200-0500 (Purpose and Statutory Authority) to 836-200-0550 (Consumer Notices to the Department), and dividing the resulting amount by the total number of filings subject to assessment between August 1 of the previous year and July 31 of the current year. The director shall determine the amount of revenue needed by considering the legislatively approved expenditures for administration of Oregon Laws 2018, chapter 7, section 2 and OAR 836-200-0500 (Purpose and Statutory Authority) to 836-200-0555 (Assessments Against Prescription Drug Manufacturers), as well as the timing of cash revenues and expenditures.
(4) The revenue collected under subsections (1) and (2) of this section must be used solely for expenses incurred in the administration of Oregon Laws 2018, chapter 7, section 2 and OAR 836-200-0500 (Purpose and Statutory Authority) to 836-200-0555 (Assessments Against Prescription Drug Manufacturers).

(5)

A manufacturer must pay each assessment imposed under this rule no later than 30 days after the date of the assessment by the department. A manufacturer must pay interest at nine percent per annum on any assessment that is not paid when due.

Source: Rule 836-200-0555 — Assessments Against Prescription Drug Manufacturers, https://secure.­sos.­state.­or.­us/oard/view.­action?ruleNumber=836-200-0555.

836‑200‑0000
Statutory Authority
836‑200‑0010
Assessments
836‑200‑0020
Filing Procedures
836‑200‑0030
Form 10 K and Other Financial Stability Filings
836‑200‑0040
Reimbursement Insurance Policy
836‑200‑0050
Registration Requirements Not Exclusive
836‑200‑0055
Annual Report
836‑200‑0060
Service on Registrant
836‑200‑0100
Notice, Collision Damage Waivers
836‑200‑0105
Statutory Authority
836‑200‑0110
Registration Procedures
836‑200‑0120
Warranty
836‑200‑0130
Reimbursement Insurance Policy
836‑200‑0140
Registration Requirements Not Exclusive
836‑200‑0200
License, Discount Medical Plan Organization
836‑200‑0210
Renewal of expired license
836‑200‑0215
One-time processing fee, cancelled application
836‑200‑0220
License Requirement Not Exclusive
836‑200‑0250
Purpose and Authority
836‑200‑0255
Registration of Contracting Entity
836‑200‑0300
Statement of Purpose
836‑200‑0305
Retainer Medical Practice Application for Certification
836‑200‑0310
Retainer Medical Practice Application for Renewal
836‑200‑0315
Disclosures
836‑200‑0401
Statement of Purpose
836‑200‑0406
Application Requirements for Pharmacy Benefit Manager
836‑200‑0411
Renewal of Pharmacy Benefit Registration
836‑200‑0416
Registration Requirements Not Exclusive
836‑200‑0421
Service on Registrant
836‑200‑0436
Submission of Complaints
836‑200‑0440
Market Conduct Requirements for Pharmacy Benefit Managers
836‑200‑0500
Purpose and Statutory Authority
836‑200‑0505
Definitions
836‑200‑0510
Account Generation Requirement
836‑200‑0515
Threshold for Reporting Drug Price Increase
836‑200‑0520
Threshold for Reporting New Specialty Drug
836‑200‑0525
Expectations of Reporting Manufacturers
836‑200‑0530
Form and Manner Requirements for Drug Pricing Reporting
836‑200‑0535
Additional Information Requests
836‑200‑0540
Information Claimed to be Trade Secret
836‑200‑0545
Public Disclosure of Prescription Drug Manufacturer Filings
836‑200‑0550
Consumer Notices to the Department
836‑200‑0555
Assessments Against Prescription Drug Manufacturers
836‑200‑0560
Civil Penalties
Last Updated

Jun. 8, 2021

Rule 836-200-0555’s source at or​.us