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It defines that the control study verifies standardized operating procedures (SOPs) produce homogeneous finished goods that meet the potency targets in the SOPs. The form details submission steps for laboratories, completion and signature requirements, legibility and “Not Applicable/NA” rules, and conditions that invalidate certification, including SOP changes and batch failures for THC or CBD.",{"@graph":69,"@context":126},[70,84,105],{"@type":71,"itemListElement":72},"BreadcrumbList",[73,77,79,82],{"item":74,"name":75,"@type":76,"position":8},"https://docshare.wps.com","Home","ListItem",{"item":78,"name":9,"@type":76,"position":14},"https://docshare.wps.com/document/",{"item":80,"name":20,"@type":76,"position":81},"https://docshare.wps.com/document/exam/",3,{"item":83,"name":65,"@type":76,"position":19},"https://docshare.wps.com/document/control-study-certification-instructions-and-sections-1-5/464103/",{"url":83,"name":65,"@type":85,"image":86,"author":91,"headline":65,"publisher":94,"fileFormat":97,"inLanguage":63,"description":67,"dateModified":98,"datePublished":99,"encodingFormat":97,"isAccessibleForFree":100,"interactionStatistic":101},"DigitalDocument",{"url":87,"@type":88,"width":89,"height":90},"https://docshare.wps.com/thumbnails/control-study-certification-instructions-and-sections-1-5/464103.png","ImageObject",300,407,{"name":92,"@type":93},"Finn","Person",{"url":74,"name":95,"@type":96},"DocShare","Organization","application/pdf","2026-10-30","2026-09-30",true,{"@type":102,"interactionType":103,"userInteractionCount":8},"InteractionCounter",{"@type":104},"ViewAction",{"@type":106,"mainEntity":107},"FAQPage",[108,114,118,122],{"name":109,"@type":110,"acceptedAnswer":111},"Who must complete and sign the certification form?","Question",{"text":112,"@type":113},"The product manufacturer completes and signs pages 1 and 2 and provides them to the laboratory when requesting compliance testing for the batch. The primary laboratory completes page 3 after testing and then submits the form to OLCC.","Answer",{"name":115,"@type":110,"acceptedAnswer":116},"What happens if the form is incomplete or illegible?",{"text":117,"@type":113},"Every section must be completed legibly. Incomplete or illegible forms are returned to the licensee and will not be reviewed by OLCC until deficiencies are corrected.",{"name":119,"@type":110,"acceptedAnswer":120},"When is a control study certification invalidated?",{"text":121,"@type":113},"Certification is invalidated if there are changes to the SOP, changes to the type of ingredient (with limited exceptions), or if a batch fails a THC or CBD test as referenced in OAR 333-007-0440(10)(b).",{"name":123,"@type":110,"acceptedAnswer":124},"How should “Not Applicable” be handled in the form?",{"text":125,"@type":113},"No blank spaces should be left. Use “Not Applicable” or “NA” in any section you believe is not applicable. If an “NA/Not Applicable” response is not appropriate, the form is returned and not reviewed until corrected.","https://schema.org",{"og:url":83,"og:type":128,"og:title":65,"og:site_name":95,"og:description":67},"article",{"robots":130,"canonical":83},"index,follow",{"doc_id":132,"site_id":62},464103,1790767681,{"code":4,"msg":5,"data":135},{"doc_id":132,"user_id":136,"nickname":92,"user_avatar":137,"doc_module":4,"category_id":19,"category_name":20,"doc_title":65,"doc_description":67,"doc_content":138,"file_id":139,"file_url":140,"file_type":141,"file_size":142,"view_count":8,"is_deleted":4,"is_public":8,"is_downloadable":8,"audit_status":8,"page_count":19,"language":143,"language_code":63,"site_id":62,"html_lang":63,"table_of_contents":144,"faqs":145,"seo_title":146,"seo_description":67,"update_tm":133,"read_time":52},34359740700684,"https://ap-avatar.wpscdn.com/avatar/1f400023980c374ae676?_k=1777273430885731487","What is this form?  \nThe purpose of a control study is to determine if a manufacturer is using standard operating procedures (SOP) that result in a finished cannabinoid concentrate, extract or product that is homogeneous , and for cannabinoid products meets the potency target identified in the SOPs.  \nThis is the form a manufacturer submits to obtain a certified control study. Manufacturers who may use this form include recreational marijuana processors, micro-tier producers with the concentrate processing endorsement, producers making kief, and hemp handler certificate holders requesting testing on products that are tracked in Metrc. Wholesalers may arrange testing on behalf of other licensees , but this form must be completed by the product manufacturer.  \nINSTRUCTIONS for completing this form:  \n􀁸 The product manufacturer completes and signs pages 1 and 2 and provide them to the laboratory when requesting compliance testing for the batch.  \n􀁸 After performing compliance testing, the primary laboratory completes page 3 , then submits the form to [OLCC.Labs@oregon.gov](OLCC.Labs@oregon.gov. Do)[. Do](OLCC.Labs@oregon.gov. Do) not provide a copy of test results or SOP unless requested. Associated test results or other documentation may be requested by the Commission to verify the responses contained in this form.  \n􀁸 Every section of this form must be completed legibly. Incomplete or illegible forms will be returned to the licensee and will not be reviewed by OLCC until deficiencies are corrected.  \n􀁸 No blanks should be left in the form. The manufacturer or laboratory representative completing this form should write “Not Applicable” or “NA” in any section they believe is not applicable to the testing of the particular product. If blank spaces are left in the form, or the Commission determines that a “Not Applicable” or “NA” response is not appropriate for a particular section, the form will be returned to the licensee and will not be reviewed by OLCC until the deficiencies are corrected.  \n􀁸 The control study is invalidated and the product manufacturer must undergo a control study for a product again or must have batches sampled and tested as if the product had not undergone a control study if:  \no There are any changes to the standard operating procedures for that product;  \no There are any changes in the type of ingredient in the product, except for a difference in the strain of usable marijuana, or the purity of an ingredient; or  \no A batch tested under the control study fails a THC or CBD test as described in OAR 333-007-0440(10)(b) .  \n􀁸 If a control study is invalidated for any reason listed in 333-007-0440(10) then a manufacturer must notify the OLCC.  \nThis form and OAR 333-007-0440 refer to standard operating procedures (SOPs) . The certification of a control study is based on the SOP and is invalidated if the manufacturer makes and changes to the SOP other than as allowed under OAR 333-007-0440(11) . Note that OLCC rules (OAR 845-025-3230) require processors to maintain written policies and procedures that include:  \n􀁸 Instructions for making each cannabinoid concentrate, extract or product;  \n􀁸 The ingredients and the amount of each ingredient for each process lot;  \n􀁸 The process for making each product;  \n􀁸 The number of servings in a process lot;  \n􀁸 The intended amount of THC per serving and in a unit of sale of the product; and  \n􀁸 The process for making each process lot homogeneous.  \nSection 1 – Business Information  \n\n| Manufacturer Name: |  |  |  |\n| --- | --- | --- | --- |\n| License or Certificate Number: |  | Email: |  |\n| Name of Manufacturer Representative Who Completed This Form: |  |  |  |\n\n\n| Section 2 – Product Information |  |  |  |  |  |\n| --- | --- | --- | --- | --- | --- |\n| Commercial Name of Item: |  |  |  |  |  |\n| Item Category: |  Concentrate (Skip Section 4) |  Extract (Skip Section 4) |  |  Cannabinoid Product (Skip Section 3) |  |\n| SOP Name or Reference: |  |  |  |  |  |\n| SOP Version","cbCaidZ6iTZIyWFu","https://ap.wps.com/l/cbCaidZ6iTZIyWFu","pdf",884559,"English","# Instructions\n## Certification and eligibility\n## Completion requirements\n## Invalidating conditions\n# Section 1 – Business Information\n# Section 2 – Product Information\n# Section 3 – Concentrate or Extract Item Information\n# Section 4 – Cannabinoid Product Item Information\n# Section 5 – Variations","[{\"question\":\"Who must complete and sign the certification form?\",\"answer\":\"The product manufacturer completes and signs pages 1 and 2 and provides them to the laboratory when requesting compliance testing for the batch. The primary laboratory completes page 3 after testing and then submits the form to OLCC.\"},{\"question\":\"What happens if the form is incomplete or illegible?\",\"answer\":\"Every section must be completed legibly. Incomplete or illegible forms are returned to the licensee and will not be reviewed by OLCC until deficiencies are corrected.\"},{\"question\":\"When is a control study certification invalidated?\",\"answer\":\"Certification is invalidated if there are changes to the SOP, changes to the type of ingredient (with limited exceptions), or if a batch fails a THC or CBD test as referenced in OAR 333-007-0440(10)(b).\"},{\"question\":\"How should “Not Applicable” be handled in the form?\",\"answer\":\"No blank spaces should be left. Use “Not Applicable” or “NA” in any section you believe is not applicable. If an “NA/Not Applicable” response is not appropriate, the form is returned and not reviewed until corrected.\"}]","Control Study Certification - Instructions and Sections 1-5 | PDF"]