Or. Admin. R. ch. 836, div. 200 – Department Regulatory Programs | Midpage

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Oregon Administrative Rules

Division 200

Or. Admin. R. ch. 836, div. 200

Department Regulatory Programs

Department of Consumer and Business Services

0000Statutory Authority; Registration; Fees; Expiration; Renewal 0010Assessments 0020Filing Procedures 0030Form 10 K and Other Financial Stability Filings 0040Reimbursement Insurance Policy 0050Registration Requirements Not Exclusive 0055Annual Report 0060Service on Registrant 0100Notice, Collision Damage Waivers 0105Statutory Authority; Registration; Fees; Expiration; Renewal 0110Registration Procedures 0120Warranty 0130Reimbursement Insurance Policy 0140Registration Requirements Not Exclusive 0200License, Discount Medical Plan Organization; Renewal 0210Renewal of expired license 0215One-time processing fee, cancelled application 0220License Requirement Not Exclusive 0250Purpose and Authority 0255Registration of Contracting Entity 0300Statement of Purpose; Authority 0305Retainer Medical Practice Application for Certification 0310Retainer Medical Practice Application for Renewal 0315Disclosures; Form and Contents 0401Statement of Purpose; Authority; Applicability 0406Application Requirements for Pharmacy Benefit Manager 0411Renewal of Pharmacy Benefit License 0416Licensure Requirements Not Exclusive 0418Aggregated Rebate and Payment Reports 0421Service on Licensee 0436Submission of Complaints 0440Market Conduct Requirements for Pharmacy Benefit Managers 0500Purpose and Statutory Authority 0505Definitions 0510Account Generation Requirement 0515Threshold for Reporting Drug Price Increase 0520Threshold for Reporting New Prescription Drug 0525Expectations of Reporting Manufacturers 0530Form and Manner Requirements for Drug Pricing Reporting 0531Prescription Drug Reporting – New Prescription Drug 0532Prescription Drug Reporting – Patient Assistance Programs 0535Additional Information Requests 0540Information Claimed to be Trade Secret 0545Public Disclosure of Prescription Drug Manufacturer Filings 0550Consumer Notices to the Department 0553Annual fees paid by drug manufacturers 0555Assessments Against Prescription Drug Manufacturers for 2023 and prior 0560Civil Penalties 0600Purpose and Statutory Authority 0605Definitions 0610License Required 0615License Application and Renewal Application 0620Licensee Reporting Requirements 0625Prohibited Conduct for Licensees 0630Civil Penalties and License Revocation 0635Education Requirements 0640Education 0645Education; Standards for Granting Credit Hours 0650Education; Education Provider Registration 0655Education; Course Registration 0660Education; Provider Trade Practices 0670Education; Credit for Unregistered Courses 0700Purpose and Scope 0705Definitions 0710Program Structure 0715Eligibility Criteria 0720Prioritization of Payments 0725Payment Structure and Limits 0730Application Process 0735Program Metrics and Reporting