Oregon Administrative Code

333-007-0310 Definitions For purposes of OAR 333-007-0300 through 333-007-0500: (1) "Added substance" means any component or ingredient added to usable marijuana, cannabinoid concentrate or cannabinoid extract during or after processing that is present in the finished cannabinoid…

333-007-0315 Ordering Tests (1) To request a compliance test a requestor must provide a laboratory, prior to laboratory taking samples, with at a minimum, the following information as applicable: (a) The registrant or licensee’s registrant or license number. (b) The name, address…

333-007-0320 Compliance Testing Requirements for Marijuana or Usable Marijuana (1) A producer or grower must test every batch from a harvest lot of marijuana or usable marijuana intended for use by a consumer or patient prior to selling or transferring the marijuana or usable mar…

333-007-0330 Compliance Testing Requirements for Cannabinoid Concentrates and Extracts (1) A processor or processing site must test every process lot of a finished cannabinoid concentrate or extract for use by a consumer or patient prior to selling or transferring the cannabinoid…

333-007-0340 Compliance Testing Requirements for Cannabinoid Products (1) A processor or processing site must test every process lot of a finished cannabinoid product intended for human consumption, use or ingestion for use by a consumer or patient prior to selling or transferrin…

333-007-0341 Compliance Testing Requirements for Finished Inhalable Cannabinoid Products (1) A processor or processing site must test every process lot of a finished inhalable Cannabinoid product prior to selling or transferring the product for the following: (a) Pesticides in ac…

333-007-0342 Compliance Testing Requirements for Industrial Hemp-Derived Vapor Items (1) Every process lot of an industrial hemp-derived vapor item for use by a consumer or patient prior to selling or transferring the item must be tested for the following: (a) Pesticides in accor…

333-007-0350 Batch Requirements for Compliance Testing (1) Marijuana or usable marijuana. (a) A producer or grower must separate each harvest lot of marijuana or usable marijuana harvested before July 1, 2022, into no larger than 15 pound batches. (b) A producer or grower must se…

333-007-0360 Sampling and Sample Size Requirements for Compliance Testing (1) Marijuana or usable marijuana. (a) Usable marijuana may only be sampled after it is cured, unless the usable marijuana is intended for sale or transfer to a processor or processing site to make a cannab…

333-007-0370 Sampling Personnel Requirements; Sampling Recordkeeping (1) Only individuals employed by a laboratory with an ORELAP accredited scope item for sampling under these rules may take samples. (2) Sampling may only be conducted at a licensee’s or registrant’s premises or …

333-007-0380 Grower and Processing Site Requirements for Labeling, Storing, and Securing Pre-Tested Marijuana Items; Recordkeeping (1) Following samples being taken from a harvest or process lot batch a grower or processing site must: (a) Label the batch with the following inform…

333-007-0390 Standards for Microbiological Contaminants Compliance Testing (1) A marijuana item or industrial hemp-derived vapor item required to be tested for microbiological contaminants under OAR 333-007-0320 to 333-007-0342 must be sampled using appropriate aseptic technique …

333-007-0400 Standards for Pesticides Compliance Testing (1) A marijuana item or industrial hemp-derived vapor item required to be tested for pesticides must be tested by a laboratory for all the analytes listed in Exhibit A, Table 3, incorporated by reference. (2) A batch fails …

333-007-0410 Standards for Solvents Compliance Testing (1) A marijuana item or industrial hemp-derived vapor item required to be tested for solvents must be tested by a laboratory for all the analytes listed in Exhibit A, Table 4 incorporated by reference. (2) A batch fails solve…

333-007-0415 Standards for Heavy Metal Compliance Testing (1) A marijuana item or industrial hemp-derived vapor item required to be tested for heavy metals must be tested by a laboratory for the analytes listed in Exhibit A, Table 8 incorporated by reference. (2) A batch fails he…

333-007-0420 Standards for Testing Water Activity and Moisture Content (1) Usable marijuana must be tested by a laboratory for: (a) Water activity; and (b) Moisture content. (2) Kief manufactured before March 1, 2023, must be tested by a laboratory for water activity unless the m…

333-007-0425 Standards for Mycotoxin Contaminants Compliance Testing (1) A marijuana item or industrial hemp-derived vapor item required to be tested for mycotoxin must be tested by a laboratory for: (a) Aflatoxins B1, B2, G1, G2; and (b) Ochratoxin A. (2) A batch fails mycotoxin…

333-007-0430 Standards for Adult Use Cannabinoid and CBD Compliance Testing (1) A laboratory must test for all of the following analytes when testing a marijuana item or industrial hemp-derived vapor item for potency: (a) Delta-9-THC. (b) Delta-9-THCA. (c) Delta-8-THC. (d) CBD. (…

333-007-0450 Failed Test Samples (1) If a sample or a duplicate sample (collectively referred to as "sample" for purposes of this rule) fails any initial test the laboratory that did the testing may reanalyze the sample. The laboratory that did the initial test may not subcontrac…

333-007-0470 Tentative Identification of Compounds (1) Tentatively Identified Compounds (TICs) are compounds detected in a sample using gas chromatography mass spectrometry that are not among the target analytes for the residual solvent analysis. (2) The Authority or Commission m…

333-007-0480 Audit and Random Testing (1) The Oregon Health Authority (Authority) may require a registrant to submit samples identified by the Authority to a laboratory of the Authority's choosing or the cannabis reference laboratory to be tested in order to determine whether a r…

333-007-0500 Quality Control and Research and Development Testing (1) A registrant or a licensee may request that a laboratory conduct testing for the purpose of assuring quality control or for research and development, except as provided in section (2) of this rule. (a) A qualit…

333-007-0600 Cannabis Reference Laboratory (1) The Oregon Health Authority (Authority) may request that the cannabis reference laboratory conduct any of the following: (a) Audit testing as described in OAR 333-007-0480; or (b) Testing if the Authority has reason to believe the ma…

333-008-0010 Definitions For the purposes of OAR chapter 333, division 8 the following definitions apply unless otherwise indicated: (1) "Advertising" means publicizing the trade name of a person responsible for a marijuana grow site (PRMG), registered processing site or dispensa…

333-008-0020 New Registry Identification Card Application Process (1) To apply for a registry identification card an individual must submit the following: (a) An application form, prescribed by the Oregon Health Authority (Authority), signed and dated by the applicant. (b) A legi…

333-008-0021 Patient and Person Responsible for a Marijuana Grow Site (PRMG) New and Renewal Fees (1) All fees referenced in this rule are non-refundable. (2) New and Renewal Application Fee. A patient must pay a $200 application fee unless the applicant qualifies for a reduced o…

333-008-0022 Proof of Residency (1) In order to be approved for a registry identification card, an applicant must be a resident of Oregon. (2) If an applicant for a registry identification card does not have a valid Oregon driver license or Oregon identification card, the applica…

333-008-0023 Patient Application Review Process (1) The Authority must review a patient application to determine if it is complete. (2) If an applicant does not provide all the information required in OAR 333-008-0020(1) or pay the applicable fee the Authority will reject the app…

333-008-0025 Person Responsible for a Marijuana Grow Site Criteria; Grow Site Registration Application Review Process (1) In order to be a PRMG an individual must: (a) Be 21 years of age or older. (b) Not have been convicted of a Class A or Class B felony under ORS 475.752 to 475…

333-008-0030 Approval of New and Renewal Patient Applications (1) If the Authority approves a patient application, the Authority shall issue a serially numbered registry identification card to the patient within five business days. (2) The registry identification card must includ…

333-008-0033 Approval of New or Renewal Person Responsible for a Marijuana Grow Site (PRMG) and Grow Site Application; Change of PRMG (1) An individual is not authorized to produce marijuana for a patient at a grow site until the Oregon Health Authority (Authority) has registered…

333-008-0035 Denial of Patient Application (1) The Authority may deny a new or renewal patient application if: (a) The applicant or patient did not provide the information required to be submitted in OAR 333-008-0020; (b) The Authority determines that the information provided was…

333-008-0037 Denial of Designation of Caregiver or Person Responsible for a Marijuana Grow Site; Denial of Grow Site Registration (1) The Authority may deny a designation of a primary caregiver made under ORS 475C.789 or an organization or facility caregiver made under ORS 475C.7…

333-008-0040 Annual Renewal (1) A patient shall register on an annual basis to maintain active registration status by submitting: (a) A renewal application prescribed by the Authority; (b) An APS signed by the patient's attending provider within 90 days prior to the expiration da…

333-008-0045 Notification of Changes (1) Patient notification responsibilities. (a) A patient must notify the Oregon Health Authority (Authority) within 10 calendar days of any change in the patient's name, mailing address, electronic mail address, telephone number, attending pro…

333-008-0047 Interim Addition or Change of Person Responsible for a Marijuana Grow Site or Grow Site Address (1) If a patient is adding a PRMG and grow site address at any time other than when applying for a new or renewal registry identification card, or if a patient is changing…

333-008-0049 Timely Submission to the Oregon Health Authority If an applicant or an individual or entity designated on an application, patient, designated primary caregiver, organization or facility caregiver or PRMG is required to submit information or documentation to the Autho…

333-008-0080 Permissible Amounts of Medical Marijuana for Patients and Caregivers (1) A patient, the patient's designated primary caregiver or organization or facility caregiver may jointly possess up to six mature marijuana plants, 12 immature marijuana plants, and 24 ounces of …

333-008-0085 Designated Primary Caregivers and Organization or Facility Caregivers (1) A designated primary caregiver may assist their patient with any matter related to the medical use of marijuana, including: (a) The production of marijuana at the address provided by the patien…

333-008-0090 Addition of Qualifying Diseases or Medical Conditions (1) For the purposes of this rule, the following definitions apply: (a) DSM means the latest published edition of Diagnostic and Statistical Manual of Mental Disorders. (b) ICD means the most recent revision of th…

333-008-0110 Oregon Cannabis Commission (1) In addition to any other duty prescribed by law, the Oregon Cannabis Commission (OCC) shall: (a) Provide advice to the Authority with respect to the administration of ORS 475C.770 to 475C.919, including rules and fees adopted and propos…

333-008-0500 Request for Grandfathered Grow Site (1) An individual or group of individuals may submit a petition, on a form prescribed by the Authority, requesting that a grow site be approved as a grandfathered grow site. (2) A petition submitted under section (1) of this rule m…

333-008-0510 Review of Petition For Grandfathered Grow Site (1) Once the Authority has determined that a petition is complete it must: (a) Conduct a criminal background check on all PRMGs listed on the application; (b) Verify that: (A) Each person listed on the application is 21 …

333-008-0520 Approval of Petition for Grandfathered Grow Site (1) The Authority will grant a petition for a grandfathered grow site if, based on the information in the petition and the Authority’s review of the petition: (a) The grow site address is currently registered with the …

333-008-0530 Denial of Petition for Grandfathered Grow Site (1) The Authority must deny a petition for a grandfathered grow site if based on the information in the petition and the Authority’s review of the petition: (a) The grow site address is not currently registered with the …

333-008-0540 Requirements for Grandfathered Grow Sites; Termination of PRMG Designation; Suspension or Revocation of PRMG Registration (1) A grandfathered grow site may only have the number of plants authorized by the Authority, based on the number of patients designating the add…

333-008-0550 General Person Responsible for a Marijuana Grow Site Requirements (1) A PRMG may not grow marijuana for more than eight patients at any one time. (2) A PRMG must display a marijuana grow site registration card at the marijuana grow site at all times for each patient …

333-008-0560 Grow Site Plant Limits (1) A PRMG may not produce more than the following per patient, subject to the overall grow site plant limits: (a) Six mature marijuana plants; (b) Twelve immature marijuana plants that are 24 inches or more in height; and (c) Thirty-six immatu…

333-008-0570 Designation of Plants at Grow Site Address (1) A person responsible for a marijuana grow site (PRMG) producing marijuana at a grow site where multiple PRMGs are registered must: (a) Physically identify the marijuana plants at a grow site that are being grown by that …

333-008-0580 Usable Marijuana Possession Limits for a Person Designated to Produce Marijuana by a Patient (1) Subject to section (2) of this rule, a person designated to produce marijuana by a patient may possess the amount of usable marijuana that the person harvests from his or…