Oregon Administrative Code

333-008-1785 Inhalable Cannabinoid Product Processing Site Requirements (1) A processing site may only use a non-cannabis additive in an inhalable cannabinoid product if the non-cannabis additive is accompanied by a list of ingredients from the manufacturer of the non-cannabis ad…

333-008-1790 Medical Marijuana Processors: Cannabinoid Edible Processor Requirements (1) A processing site endorsed to make cannabinoid edibles may only process in a food establishment licensed by the Oregon Department of Agriculture (ODA) and must comply with the applicable prov…

333-008-1800 Medical Marijuana Processors: Cannabinoid Concentrate and Extract Processor Requirements (1) Cannabinoid Concentrates or Extracts. A processing site endorsed to make cannabinoid concentrates or extracts: (a) May not use Class I solvents as those are classified in the…

333-008-1810 Medical Marijuana Processors: Cannabinoid Topical, Tincture, Capsule, Suppository or Transdermal Patch Processor (1) A processing site endorsed to make cannabinoid topicals, tinctures, capsules, suppositories or transdermal patches may not engage in processing in a l…

333-008-1820 Medical Marijuana Processors: Registered Processing Site Recordkeeping (1) In addition to other record keeping required in these rules a registered processing site must keep records documenting the following: (a) How much marijuana is in each process lot, as that ter…

333-008-1835 Medical Marijuana Processors: Processing Site CTS Tracking (1) All registered processing sites must track the transfers of marijuana, usable marijuana, medical cannabinoid products, cannabinoid concentrates and cannabinoid extracts to and from the processing site in …

333-008-2000 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Definitions For purposes of OAR 333-008-2000 to 333-008-2200: (1) "Applicant" means a person applying for a new or renewal registration for a dispensary or processing site. (2) "Registrant"…

333-008-2010 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Communication with the Oregon Health Authority If an applicant or registrant is required to or elects to submit information or documentation to the Authority by a particular deadline it mus…

333-008-2020 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Criminal Background Checks (1) An individual named in a new or renewal application as required by OAR 333-008-1020 or 333-008-1620, or if otherwise required by these rules, must provide to …

333-008-2030 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Notification of Changes (1) A registrant must notify the Oregon Health Authority (Authority) within 10 calendar days of any of the following: (a) The conviction for the manufacture or deliv…

333-008-2040 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Changing, Altering, or Modifying Licensed Premises (1) A registrant may not make any physical changes to the premises that materially or substantially alters the premises or the usage of th…

333-008-2050 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Change in Location (1) A registrant that wishes to change its location must submit a new application that complies with OAR 333-008-1020 or 333-008-1620. (2) A registrant may not operate at…

333-008-2060 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Secretary of State Registration Required A registrant must maintain a current registration as a business with the Office of the Secretary of State in order to receive or maintain registrati…

333-008-2070 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Advertising Restrictions (1) A registrant may not have advertising that: (a) Contains statements that are deceptive, false, or misleading; (b) Contains any content that can reasonably be co…

333-008-2080 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Security Requirements In order to be registered and remain registered a registrant must: (1) Have an installed and fully operational security alarm system, installed by an alarm installatio…

333-008-2090 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Video Surveillance Equipment In order to be registered and remain registered a registrant must: (1) Have an installed and fully operational video surveillance recording system with video su…

333-008-2100 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Required Camera Coverage and Camera Placement In order to be registered and remain registered a registrant must: (1) Have security camera coverage for: (a) All secure and limited access are…

333-008-2110 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Video Recording Requirements (1) In order to be registered and remain registered a registrant must: (a) Have cameras that are installed, operational, and continuously record 24 hours a day …

333-008-2120 General Requirements for Medical Marijuana Processing Sites and Dispensaries Location and Maintenance of Surveillance Equipment (1) A registrant must: (a) Have the surveillance recording equipment housed in a designated secure area or other locked enclosure with acce…

333-008-2140 General Requirements for Medical Marijuana Processing Sites and Dispensaries: State and Local Safety Inspections (1) A registered premises may be subject to inspection by state or local government officials to determine compliance with state or local health and safet…

333-008-2150 General Requirements for Medical Marijuana Processing Sites and Dispensaries: General Sanitary Requirements (1) A registrant must: (a) Prohibit any individual working on the registered premises who has or appears to have a communicable disease, open or draining skin …

333-008-2160 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Foreclosure; Cessation of Operations In the event that a registrant is foreclosed or otherwise ceases operations as described in ORS chapter 79, a secured party, as defined in ORS 79.0102, …

333-008-2170 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Inspections (1) The Authority must conduct a routine inspection of every registrant at least every year. (2) The Authority may conduct a complaint inspection at any time following the recei…

333-008-2180 Violations (1) It is a violation for an applicant for a registration, registrant or registrant representative to: (a) Fail to cooperate with an inspection or investigation by the Oregon Health Authority (Authority) or the Oregon Liquor and Cannabis Commission (Commis…

333-008-2190 General Requirements for Medical Marijuana Processing Sites and Dispensaries Enforcement (1)(a) Informal Enforcement. If, during an inspection the Oregon Health Authority (Authority) documents violations of ORS 475C.815 to 475C.827, 475C.833 to 475C.843, 475C.544, 47…

333-008-2200 General Requirements for Medical Marijuana Processing Sites and Dispensaries: Civil Penalties (1) In addition to any other liability or penalty provided by law, the Authority may impose, against any person, a civil penalty that does not exceed $500 per day, for each …

333-008-2210 Penalty Matrix (1) The penalty matrix applies to any violations in OAR chapter 333, division 7 and 8. (2) The Authority has established Category I, II, III and IV violations with Category I violations posing the highest risk to public health and safety, and category …

333-008-3000 Medical Marijuana Records: Medical Marijuana Confidentiality The Oregon Health Authority may only disclose identifying information concerning applicants or registrants in accordance with the following statutes, unless otherwise required by law: (1) ORS 475C.856 (Data…

333-008-3010 Medical Marijuana Records: System to Allow Verification of Data at All Times By State and Local Law Enforcement (1) The Authority shall establish an interactive method to allow authorized employees of state and local law enforcement agencies to use the Oregon State P…

333-008-5000 Product Recall (1) The Oregon Health Authority (Authority) may request or require a patient, caregiver, person responsible for a marijuana grow site (PRMG), dispensary, or processing site to recall any marijuana item that they have sold or transferred that does not m…

333-009-0000 Definitions For the purpose of OAR 333-009-0000 through 333-009-0030, the following definitions apply. (1) "Act" means the "Oregon Death with Dignity Act" or Measure 16 as adopted by the voters on November 8, 1994. (2) "Adult" means an individual who is 18 years of a…

333-009-0010 Reporting (1) To comply with ORS 127.865(2), within seven calendar days of writing a prescription for medication to end the life of a qualified patient the attending physician shall send the following completed, signed and dated documentation by regular mail to the S…

333-009-0020 Record Review/Annual Report (1) The Authority shall annually review records maintained pursuant to this Act. (2) The Authority shall generate and make available to the public an annual statistical report of information collected under this Act. Statutory/Other Author…

333-009-0030 Confidentiality/Liability (1) All information collected pursuant to ORS 127.800 to 127.897 including, but not limited to, the identity of patients, physicians and other health care providers, and health care facilities shall not be a public record and may not be made…

333-010-0000 Cancer Reporting Regulations: Definitions (1) "Active follow-up program" means a program for a health care facility to determine, at least annually, information including but not limited to the vital status of each case. (2) "Admitted" means a rendering of any servic…

333-010-0020 Cancer Reporting Regulations: Reporting Requirements for Health Care Facilities This rule describes the specific requirements for health care facilities. Such facilities include inpatient facilities, outpatient facilities acting under the license of a hospital, ambul…

333-010-0030 Cancer Reporting Regulations: Reporting Requirements for Practitioners (1) Any practitioner diagnosing a case of reportable cancer or a reportable non-malignant condition, as defined in OAR 333-001-0000(16) and 333-010-0000(18) respectively, must notify OSCaR of each…

333-010-0032 Cancer Reporting Regulations: Reporting Requirements for Clinical Laboratories (1) Clinical laboratories must report to OSCaR all cases with test results indicative of and specific for a reportable cancer or reportable non-malignant condition, as defined in OAR 333-0…

333-010-0035 Cancer Reporting Regulations: Patient Notification Requirement This rule describes the process for notifying patients that information about a reportable cancer has been reported to OSCaR. (1) OSCaR may, but is not required to notify patients that information about a…

333-010-0040 Cancer Reporting Regulations: Quality Standards The usefulness of OSCaR data is directly dependent upon the accuracy, completeness, and timeliness of the data available in its database. ORS 432.510 directs the Oregon Health Authority to establish a quality control sy…

333-010-0050 Cancer Reporting Regulations: Confidentiality and Access to Data This rule describes when confidential and privileged information collected and maintained by OSCaR may be shared and the process for obtaining aggregate non-confidential OSCaR information that is not pu…

333-010-0055 Cancer Reporting Regulations: Research Studies (1) Requirements for Research Studies. Before any confidential data may be disclosed to a researcher, OSCaR must: (a) Approve a submitted protocol for the proposed research, which describes how the research will be used …

333-010-0060 Cancer Reporting Regulations: Special Studies (1) From time to time, OSCaR may elect to conduct special studies of cancer mortality, morbidity, treatment options and cancer control. OSCaR is specifically authorized to obtain any information which may apply to a patie…

333-010-0070 Cancer Reporting Regulations: Advisory Committee The Authority shall appoint an advisory committee to review the operations of the central registry and to make recommendations regarding registry policy, and to review research protocols for which confidential and priv…

333-010-0080 Cancer Reporting Regulations: Training and Consultation The Authority shall provide annual continuing education for interested persons involved in cancer registry reporting. Continuing education content must include, but is not limited to, cancer diagnosis and manage…

333-010-0090 Cancer Reporting Regulations: Fees This rule describes the process by which the Authority will calculate the cost of providing cancer reporting services to health care facilities, practitioners or clinical laboratories. For health care facilities, practitioners and c…

333-010-0100 ScreenWise Breast and Cervical Cancer Program: Description of the ScreenWise Breast and Cervical Cancer Program The mission of the Oregon ScreenWise Program is to reduce breast cancer, cervical cancer, cardiovascular disease and other diseases by promoting early dete…

333-010-0105 Definitions (1) "Agency number" means the administrative number assigned to the service provider by the Center for Prevention and Health Promotion (Center) for identification as a ScreenWise Breast and Cervical Cancer services (ScreenWise BCC) provider. (2) "Ancillar…

333-010-0110 Client Eligibility In order to be eligible for the ScreenWise BCC a client must meet the following eligibility criteria: (1) Have an income based on family size that is at or below 250 percent of the Federal Poverty Level at the time of enrollment; and (2) Reside or …

333-010-0115 Client Enrollment (1)(a) Clients are determined eligible on a self-declared basis, when they submit a completed and signed ScreenWise BCC enrollment form at the clinic site at the time of service. (b) Prior to enrolling a client in ScreenWise BCC, providers with acce…