1. (1) A manufacturer must provide to a laboratory, prior to the laboratory taking samples, the following information:

   1. (a) The manufacturer’s license number and endorsement type;
   2. (b) The manufacturer’s name, address and contact information;
   3. (c) Type of psilocybin product;
   4. (d) Unique identification numbers assigned to products that will be sampled;
   5. (e) Total mass or volume of each batch to be sampled; and
   6. (f) Identification of tests requested pursuant to OAR 333-333-7030, OAR 333-333-7040, OAR 333-333-7050, OAR 333-333-7060, OAR 333-333-7070, OAR 333-333-7080 and OAR 333-333-7150.
2. (2) If the manufacturer informs a laboratory that a psilocybin product is being re-sampled after a failed test, the manufacturer must provide the laboratory with documentation of the failed test.
3. (3) A manufacturer is responsible for ordering the compliance tests necessary to comply with OAR 333-333-7010 to OAR 333-333-7150.
4. (4) A manufacturer may not order more than one compliance test for the same harvest lot, process lot or psilocybin product except as allowed under OAR 333-333-7120.

5. (5) A manufacturer violates these rules if they:

   1. (a) Fail to provide information required in these rules to a laboratory.
   2. (b) Submit false or misleading information to a laboratory.
6. (6) Tests ordered under these rules expire after one year. If a test has expired, the psilocybin product must be tested again before it can be sold to a client, transferred to another licensee, or converted to another product type.
7. (7) Manufacturers may only order tests for the purposes described in OAR 333-333-7010 to OAR 333-333-7150.

Statutory/Other Authority

ORS 475A.235 & ORS 475A.590

Statutes/Other Implemented

ORS 475A.235 & ORS 475A.590

History

PH 82-2024, amend filed 11/22/2024, effective 01/01/2025
PH 58-2023, amend filed 12/21/2023, effective 01/01/2024
PH 74-2022, adopt filed 05/19/2022, effective 05/20/2022