OAR 333-333-7040: Potency Testing
Edition: Current OARD snapshotEffective: 2024-01-01Last verified: 2026-09-07
(1) A manufacturer must order tests for every batch of finished psilocybin product from a harvest lot or process lot to determine the concentration (potency) of psilocybin and psilocin in the product. (2) A process lot of homogenized fungi, psilocybin extract or edible psilocybin product fails potency testing if the amount of psilocybin or psilocin between primary and duplicate samples taken from the batch exceeds 20 percent relative percent difference between samples. (3) In addition to the requirements of section (1) of this rule, a manufacturer must submit one or more batches from a harvest lot or process lot for potency testing upon written request by the Oregon Health Authority.
Official history and status
Statutory/Other Authority: ORS 475A.235 & ORS 475A.590
Statutes/Other Implemented: ORS 475A.235 & ORS 475A.590
History: PH 58-2023, amend filed 12/21/2023, effective 01/01/2024 PH 74-2022, adopt filed 05/19/2022, effective 05/20/2022
This rule cites
- section (1) of this rule — target_record_not_published
Cited by
- OAR 333-064-0140: Psilocybin Products Sampling Procedures and Testing
- OAR 333-064-0150: Reporting Psilocybin Products Test Results
- OAR 333-333-1010: Definitions
- OAR 333-333-2200: Psilocybin Product Quantity Limits
- OAR 333-333-2400: Labeling for Sale to Client
- OAR 333-333-2410: Product Information Document
- OAR 333-333-6030: Laboratory Licensee Prohibited Conduct
- OAR 333-333-7020: Ordering Tests
- OAR 333-333-7100: Psilocybin Product Sampling Requirements
- OAR 333-333-7120: Failed Test Samples
Official source: https://secure.sos.state.or.us/oard/