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Bill C-286 (Thomas’ Bill) explained: what it would change

Topic: Law and policy in Canada

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Short answer, checked 4 October 2026

Bill C-286, known as Thomas’ Bill, is a private member’s bill introduced on 16 June 2026 by Conservative MP Corey Tochor. Its text would treat psilocin and psilocybin differently under two sets of federal rules and would deem some priority-review requests for them to be granted. As of 4 October 2026 it has had first reading only: no second reading, no votes and no committee study. It is not law.

On this page 11 sections

People searching for Bill C-286 are usually asking one of three things: what it says, whether it has passed, and whether it makes magic mushrooms legal. This article answers those from the primary record: the bill’s own text, the LEGISinfo page run by Parliament, and the House of Commons debates of the day it was introduced. It takes no side. It does not predict what will happen to the bill.

General information, not legal advice

This article explains a bill and the law around it. It is not legal advice, and it is not medical advice. Laws, regulations and bills change, and how they apply to a real situation is a question for a lawyer. Check the current position on the official pages: LEGISinfo, Health Canada’s page on psilocybin and the Controlled Drugs and Substances Act on Justice Laws. For safety information, see our safety page. In an emergency, call 911 or your local emergency number, or your poison control centre.

What is Bill C-286, and who introduced it?

Bill C-286 is a private member’s bill in the 45th Parliament, first session. Its long title is “An act to amend the Controlled Drugs and Substances Act and the Food and Drugs Act”. LEGISinfo lists Corey Tochor as its sponsor. He is a Conservative MP from Saskatoon: LEGISinfo gives his riding as Saskatoon East, while the House debates of the day name it Saskatoon—University (LEGISinfo; Hansard, 16 June 2026).

The bill has no official short title in the published text. “Thomas’ Bill” is the name the sponsor used at introduction: he called it Thomas’s bill and said Thomas was a constituent who had stage 4 cancer (Hansard). A website titled Thomas’ Bill links to the bill. We cite it only for the name; the claims on it are advocacy, and we have not repeated them.

In his remarks the sponsor said that Thomas’s doctor prescribed psilocybin with counselling, that Thomas obtained it through Health Canada’s special access program, and that it was working for three years until he was cut off. These are the sponsor’s statements in the House. We have not verified them. He described the bill’s aim as letting physicians prescribe psilocybin counselling to patients without Health Canada overriding them (Hansard). The same entry in the debates records Elizabeth May, a Green MP, saying she would support it.

Do not confuse this bill with others that share the number. Bill numbers are reused in each session, and earlier Parliaments had unrelated bills numbered C-286 (openparliament.ca). The one discussed here is C-286 in the 45th Parliament, 1st session.

What does the text of Bill C-286 say?

The first-reading text is short: a purpose clause and three amending clauses. The table sets out what each clause provides, with our plain reading beside it. Both are our summaries, so read the bill itself before relying on either. We cross-checked it against the XML version Parliament publishes (bill XML).

Bill C-286 as introduced on 16 June 2026: clause by clause
ClauseWhat the text providesPlain reading (ours)
SummaryThe enactment amends the two Acts to allow psilocin and psilocybin to be used for medical treatment in accordance with the Narcotic Control Regulations. It also provides for automatic approval of requests for priority review for certain new drugs.The official summary of the bill’s purpose. It is part of the bill as printed but is not an operative clause.
1 (purpose)States the Act’s purpose as improving access to hallucinogenic drug medical treatment and not circumventing existing approval processes for new drugs.Two aims side by side: wider medical access, and no bypass of the new-drug approval process.
2 (Controlled Drugs and Substances Act, new subsections 2(4) and 2(5))For the purposes of the Narcotic Control Regulations, “narcotic” would mean psilocin and psilocybin and their salts, a controlled substance in that regulation’s schedule, or, for a midwife, nurse practitioner or podiatrist, a scheduled substance they may prescribe, possess or deal with under the New Classes of Practitioners Regulations. For the purposes of Part J of the Food and Drug Regulations, “restricted drug” would mean a substance in that Part’s schedule other than psilocin or psilocybin or their salts.Moves psilocin and psilocybin out of the restricted-drug category and into the narcotic category, but only “for the purposes of” those two named regulations.
3 (Food and Drugs Act, section 2)Renumbers section 2 as subsection 2(1) and adds subsection 2(2), repeating the same “restricted drug” definition for Part J of the Food and Drug Regulations.The same exclusion, written into the second Act.
4 (Food and Drugs Act, new section 15.1)A request for priority review status on a new drug submission, made under the department’s Priority Review of Drug Submissions Policy, is deemed granted on the day the department receives it if the request concerns psilocin, psilocybin, their salts, or any substance with a substantially similar chemical structure.Priority-review status would follow automatically from the request. The clause says nothing about whether the drug is then approved.

Where is Bill C-286 now?

As of 4 October 2026, LEGISinfo shows first reading as the latest completed stage, on 16 June 2026. Second reading, consideration in committee, report stage, third reading and all Senate stages are marked “not reached”. The record lists no House votes and no committee meetings, and no royal assent. LEGISinfo’s status line reads “Outside the Order of Precedence” (LEGISinfo record).

First reading of a private member’s bill is a formality. In the debates of 16 June, the motions were deemed adopted and the bill was read the first time and printed (Hansard). The House of Commons explains that private members’ bills are debated through an order of precedence built from a random draw of members’ names, and that items on it are considered in the order listed, usually one a day (House of Commons procedure). A bill outside that order is not on that list. That is what the LEGISinfo status line says about C-286. What happens next depends on parliamentary procedure and decisions we cannot see, and we make no forecast.

For comparison, a different private member’s bill about special access to drugs, Bill C-265 (sponsor: Marcus Powlowski), has passed second reading and been referred to committee (LEGISinfo, C-265). We checked the bill’s text: it does not mention psilocybin. It is a separate bill from C-286.

How does federal law treat psilocybin today?

To see what C-286 would change, it helps to see the current rules. The Controlled Drugs and Substances Act lists psilocin and psilocybin in Schedule III, and says that, except as authorized under the regulations, no person shall possess a Schedule III substance (Justice Laws, CDSA). Health Canada says the production, sale and possession of magic mushrooms are illegal in Canada, and that there are no approved therapeutic products containing psilocybin in Canada or elsewhere (Health Canada). Our deeper explainer is are magic mushrooms legal in Canada?.

Two routes exist for medical or scientific use. First, the Minister of Health can exempt a person, a class of persons or a substance from the Act for a medical or scientific purpose or in the public interest, under section 56(1) (Justice Laws, CDSA). See section 56 exemptions and psilocybin. Second, the Special Access Program lets a licensed practitioner request access to a drug that is not authorized for sale. Health Canada says it reviews requests case by case, only practitioners (not patients) can apply, and an authorization is not a statement that a drug is safe or effective (Health Canada SAP notice, 27 February 2023; Health Canada). More in the special access program and psilocybin.

How the regulations sort psilocybin is the key background for the bill. Health Canada’s SAP notice calls psilocybin and MDMA restricted drugs. The new Controlled Substances Regulations (SOR/2025-242) came into force on 1 October 2026 (Canada Gazette; Ontario College of Pharmacists, 1 October 2026). They list psilocin and psilocybin in Schedule 4, Part 1, the restricted drugs. They define a prescription as an authorization for a controlled substance other than a restricted drug, and let a practitioner named in a letter of authorization, issued under section C.08.010 of the Food and Drug Regulations, possess a restricted drug (Canada Gazette). In short, restricted drugs reach patients through a letter of authorization, not an ordinary prescription.

A typed letter at the centre of a clinic desk, a small blank notepad pushed aside and a stethoscope nearby.
Under the new regulations, psilocin and psilocybin are restricted drugs, which reach patients through a letter of authorization rather than an ordinary prescription.Illustration by Shroomverse, AI-generated.

What would Bill C-286 change if it passed?

Taking the text as introduced, its operative effects are of three kinds. None is certain; how a court or Health Canada would apply the wording is a legal question, and bills can be amended before they pass.

  • Category. The text says that for the Narcotic Control Regulations psilocin and psilocybin count as narcotics, and that for Part J of the Food and Drug Regulations they are not restricted drugs. In the Acts we searched, current to 21 September 2026, neither “narcotic” nor “restricted drug” is defined; the bill would add those definitions to the Controlled Drugs and Substances Act and the Food and Drugs Act (CDSA; Food and Drugs Act).
  • Priority review. Any request for priority review of a new drug submission for psilocin, psilocybin or a substantially similar substance would be deemed granted on the day it is received. Health Canada’s guidance says priority review means a 180-day review target, compared with 300 days for non-priority submissions (Health Canada fact sheet). It sets eligibility criteria: a serious, life-threatening or severely debilitating condition with substantial evidence of clinical effectiveness, plus either an unmet need or an improved benefit-risk profile. The sponsor must send a written request and a clinical assessment package before filing the submission, and Health Canada says it will tell the sponsor within 30 calendar days whether the request is accepted (Health Canada guidance). The bill’s deeming rule would replace the department’s decision about that request for these substances.
  • Stated purpose. The bill’s purpose clause would put into the statute that the aim is access to hallucinogenic drug medical treatment without bypassing existing approval processes.

The sponsor’s stated aim in the House was to let physicians prescribe psilocybin counselling without Health Canada overriding them (Hansard). Whether the text’s wording achieves that is a question for lawyers and for the committee stage, if the bill reaches one. We do not assess it.

What would Bill C-286 not change?

  • Magic mushrooms. The text names psilocin and psilocybin and their salts. It does not mention mushrooms, and it does not change the Health Canada position that production, sale and possession of magic mushrooms are illegal (bill text; Health Canada).
  • The schedules and offences. The bill amends section 2 of the Controlled Drugs and Substances Act and adds definitions. It does not amend Schedule III or the possession and trafficking offences (bill text).
  • Drug approval. The text does not approve any psilocybin product. Health Canada says no therapeutic product containing psilocybin is approved in Canada (Health Canada), and the bill’s own purpose clause says it is not meant to circumvent approval processes. Priority review shortens a review target; it is not an approval.
  • Practice rules. The text says nothing about training, facilities, doses, who may be treated or what a clinician must do. We found no provisions of that kind in it.

The text contains no provision about a patient’s entitlement to psilocybin, and none about possession by members of the public.

Does the bill match the regulations in force on 4 October 2026?

This is a drafting observation, and it is confirmed by the regulation’s own text. The bill’s text relies on the Narcotic Control Regulations, Part J of the Food and Drug Regulations and, in clause 2, the New Classes of Practitioners Regulations. The Controlled Substances Regulations repeal all three: section 237 repeals Part J (with Part G) of the Food and Drug Regulations, section 238 repeals the Narcotic Control Regulations and the New Classes of Practitioners Regulations (among others), and section 239 sets the coming into force for 1 October 2026 (Canada Gazette). The Ontario College of Pharmacists stated on 1 October 2026 that the regulations are in effect (OCP).

The Shroomverse alien at a reading table in the round, domed Library of Parliament, holding a printed document beside three booklets tied with string.
The bill’s text relies on three sets of regulations that the new Controlled Substances Regulations repeal, with effect from 1 October 2026.Illustration by Shroomverse, AI-generated.

The Justice Laws consolidations we opened are current to 21 September 2026, before that date, and so still show the Narcotic Control Regulations (Justice Laws, NCR; Justice Laws, CSR). The bill was printed on 16 June 2026, before the 1 October date. The bill as introduced therefore refers to regulations that, from 1 October 2026, are no longer in force. We cannot say how Parliament, Health Canada or a court would read the bill against the new regulations, or whether the text would be amended. If you rely on it, check the current text on LEGISinfo.

A smaller point is the date in clause 4, which refers to a Priority Review of Drug Submissions Policy “adopted by the Department on December 13, 1996”. Health Canada’s guidance explains both dates. Its background section says that on 13 December 1996 the former Therapeutic Products Programme issued a policy statement titled Priority Review of Drug Submissions. The guidance document’s own control block gives 16 September 2002 as the date adopted, 30 November 2005 as the revised date, 1 March 2006 as the effective date and 18 December 2008 as the administrative-changes date (Health Canada guidance). So 1996 is the date of the original policy statement, and 2002 is the adoption date of the guidance as it now stands. The bill’s “as amended from time to time” wording would apply to the current version; we do not interpret how.

What has Health Canada said about it?

We found no Health Canada or ministerial statement about Bill C-286 itself. What Health Canada has published are statements about the present system: its psilocybin page (modified 20 October 2026) says clinical trials are the most appropriate way to advance research with unapproved drugs, that no approved therapeutic products contain psilocybin, and that the Special Access Program and section 56(1) exemptions are case-by-case routes (Health Canada). Its Special Access Program notice (27 February 2023) says requests are reviewed case by case and that a practitioner must supply evidence for the patient’s condition (Health Canada SAP notice). These are statements about the law as it stands, not responses to the bill.

Health Canada’s regulatory impact statement for the Controlled Substances Regulations also says the regulations incorporate the earlier class exemption that covered activities with psilocybin and MDMA in relation to a Special Access Program authorization (Canada Gazette).

How can I follow Bill C-286?

What we could not verify

  • The account of Thomas’s treatment: it is the sponsor’s own statement in the House, and we did not check it.
  • How the bill’s wording would work in practice, now that the regulations it names have been repealed from 1 October 2026.
  • Any statement by Health Canada or the Minister about this bill.

Common questions

What is Bill C-286?

A private member’s bill, introduced on 16 June 2026 by Conservative MP Corey Tochor in the 45th Parliament, first session. It would amend the Controlled Drugs and Substances Act and the Food and Drugs Act in relation to psilocin and psilocybin. It is also called Thomas’ Bill.

Has Bill C-286 passed?

No. As of 4 October 2026, LEGISinfo shows only first reading, completed on 16 June 2026. It lists no second reading, no votes, no committee study and no Senate stages. It has not received royal assent and is not law.

Would Bill C-286 make magic mushrooms legal?

Its text does not mention mushrooms and does not amend the schedules or offences in the Controlled Drugs and Substances Act. It deals with how psilocin and psilocybin are classed under two named sets of regulations and with priority review. Health Canada says production, sale and possession of magic mushrooms are illegal.

Why is it called Thomas’ Bill?

The sponsor introduced it in the House as Thomas’s bill, naming a constituent who had stage 4 cancer. The published bill has no official short title. LEGISinfo lists it only by its long title.

What does priority review mean in the bill?

Health Canada’s priority review gives a new drug submission a 180-day review target instead of 300 days. Under the bill, a request for priority review on a psilocybin or psilocin submission would be deemed granted when received. That changes the review timeline, not whether a drug is approved.

Can I get psilocybin through the Special Access Program today?

Health Canada says only licensed practitioners, not patients, can request access, that each request is reviewed case by case, and that there is no guarantee of approval. This is general information, not medical or legal advice. See our special access program article and speak to a health professional.

Is this article legal advice?

No. It summarizes a bill and public sources as of 4 October 2026. Laws and bills change, and how they apply to your situation is a question for a lawyer. For safety information see our safety page.

Shroomverse sells mushroom products. This article is general information about a federal bill and the law around it. It is not legal or medical advice, and it does not encourage anyone to use drugs.

SOURCES

  1. Bill C-286 (45-1), An act to amend the Controlled Drugs and Substances Act and the Food and Drugs Act, Parliament of Canada, LEGISinfo. Accessed . Sponsor, status “Outside the Order of Precedence”, first reading on 16 June 2026 as the latest completed stage, later stages not reached.
  2. LEGISinfo data record for Bill C-286 (45-1), Parliament of Canada, LEGISinfo (JSON feed). Accessed . Read in full: no House or Senate votes, no committee meetings, no royal assent, sponsor’s riding (Saskatoon East) and the dates of each stage.
  3. Bill C-286, first reading text (45th Parliament, 1st session), Parliament of Canada, DocumentViewer. Accessed . Summary and clauses 1 to 4.
  4. Bill C-286, first reading, English XML, Parliament of Canada. Accessed . Full text read; used to confirm the wording of the clauses and that there is no official short title.
  5. House of Commons Debates (Hansard), vol. 152, no. 137, 16 June 2026, House of Commons of Canada. Accessed . Introduction and first reading of C-286; the sponsor’s remarks on Thomas and the bill’s aim; the Elizabeth May exchange; the sponsor’s riding as named in the debates.
  6. Bill C-286, openparliament.ca, openparliament.ca. Accessed . Secondary source: status, the reuse of the number C-286 in earlier Parliaments, and a transcript of the first-reading remarks.
  7. Thomas’ Bill, Website titled Thomas’ Bill (links to C-286 on LEGISinfo). Accessed . Cited only for the name “Thomas’ Bill” and for the page linking to the bill. It is an advocacy page; its claims were not used.
  8. How Private Members’ Bills Get Debated, House of Commons of Canada, Procedure and Practice. Accessed . The random draw, the order of precedence, one item considered per day, and the two hours of debate at second reading.
  9. Bill C-265 (45-1), An Act to amend the Food and Drugs Act (List of Therapeutic Products Pre-approved for Special Access), Parliament of Canada, LEGISinfo (JSON feed). Accessed . Sponsor, stage (second reading and referral to committee on 10 June 2026) and a text search showing no mention of psilocybin.
  10. Controlled Drugs and Substances Act, S.C. 1996, c. 19 (current to 2026-09-21), Justice Laws Website. Accessed . Schedule III items 11 and 12 (psilocin, psilocybin); section 4(1) possession; section 56(1) exemptions; no definition of “narcotic” or “restricted drug” in the Act text.
  11. Food and Drugs Act, R.S.C. 1985, c. F-27 (current to 2026-09-21), Justice Laws Website. Accessed . Searched for a definition of “restricted drug”; none found in the Act text.
  12. Controlled Substances Regulations, SOR/2025-242, Canada Gazette, Part II, 17 December 2025. Accessed . Sections 237 to 239 (repeals; coming into force on 1 October 2026); Schedule 4, Part 1 items 8 and 9 (psilocin and psilocybin as restricted drugs); the definitions of “prescription” and “letter of authorization” (section C.08.010 of the Food and Drug Regulations); section 6 on possession of restricted drugs; the regulatory impact statement on the psilocybin and MDMA class exemption.
  13. New Controlled Substances Regulations now in effect (1 October 2026), Ontario College of Pharmacists. Accessed . Statement that the Controlled Substances Regulations are in effect as of 1 October 2026.
  14. Controlled Substances Regulations (SOR/2025-242), consolidated, Justice Laws Website. Accessed . Consolidation current to 2026-09-21.
  15. Narcotic Control Regulations (C.R.C., c. 1041), consolidated, Justice Laws Website. Accessed . Consolidation current to 2026-09-21, last amended 2024-06-05; the regulation is still shown there.
  16. Psilocybin and psilocin (magic mushrooms) (page modified 20 October 2026), Health Canada. Accessed . Re-read 24 October 2026. Illegality of magic mushrooms; no approved therapeutic products; clinical trials; Special Access Program; section 56(1) exemptions.
  17. Notice to stakeholders: Requests to the Special Access Program (SAP) involving psychedelic-assisted psychotherapy (27 February 2023), Health Canada. Accessed . Who may request, case-by-case review, evidence required, no broad statement that a drug is safe or effective, psilocybin classed as a restricted drug.
  18. Guidance for Industry: Priority Review of Drug Submissions, Health Canada. Accessed . Eligibility criteria, written request and clinical assessment package, 30-day decision notice, 180-day target; section 1.2 on the 13 December 1996 policy statement; control block: adopted 2002/09/16, revised 2005/11/30, effective 2006/03/01, administrative changes 2008/12/18.
  19. Priority Review of Drug Submissions (Therapeutic Products) fact sheet (page modified 2017-05-04), Health Canada. Accessed . 180-day target versus 300 days for non-priority; the page gives no adoption date for the policy.

CHANGES

  • : Published.
  • : Re-read Health Canada’s psilocybin page, updated on 20 October 2026, and corrected its date here. The statements this article cites from it are unchanged.

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