New Mexico Medical Psilocybin Program · Advisory Board

The controlled-substance number: the certifying-clinician access point

Updated July 25, 2026. The requirement is in the July 23 published proposed rule, which goes to a rule hearing on August 28, 2026.

The “certifying clinician” is the person who certifies a patient into the program. The published rule requires that clinician to hold a New Mexico controlled-substance number, in two places: the clinician’s own application packet must contain it (7.35.3.9 (D)(2), p. 3), and every patient’s enrollment application must record it (7.35.3.8 (B)(3), p. 1). The July 9 Advisory Board sent the requirement back to the department; on July 17 the department said it would keep it, and the rule published on July 23 does. What stands now, and what is still open, is in the update below.

Through July 23, 2026

Where the requirement stands now

At the July 17 Advisory Board meeting the department said it would keep the controlled-substance-number requirement, and gave revised language for how the certifying clinician evaluates a patient. The rule published six days later carries both: the number at 7.35.3.9 (D)(2), p. 3 and 7.35.3.8 (B)(3), p. 1, and the evaluation language at 7.35.3.13 (A), p. 8.

The requirement stays, and is going into the rule. Dominic Zurlo (director, NM DOH Center for Medical Cannabis and Psilocybin) said that after taking the earlier concerns to the Secretary of Health and consulting the department’s attorneys, the controlled-substance-number requirement will remain in the rule the department puts forward. In his words: “this being a medical program that is going to be a requirement that the department is putting forward,” and, after taking the concerns back, “the department at least is going to move forward from a regulatory standpoint with that as a requirement.” He described it as consistent with the medical cannabis program, where a certifying clinician has always had to hold the number, and said it has to apply across the board rather than only for certain conditions or higher-risk patients. The board did not vote to remove it.

Why the department says it is needed. Zurlo noted that psilocybin remains a Schedule I substance, set aside for program use rather than rescheduled, and that although the certification is not a prescription it is treated like one for a medical program, the same as medical cannabis. Dr. Robert Truckner (department medical director) added that the medicine itself is considered safe, but the concern is the health status of patients, who he expects will carry higher illness burdens.

The state number, not a federal DEA license. The requirement is the New Mexico controlled-substance number; the department said the proposed rule does not separately require a federal DEA license. How the state number relates to a DEA license was not settled at the meeting: some found the state application asks for no DEA license, while others said a DEA license is needed to obtain or keep one over time. The department is checking with the Board of Pharmacy. Only about three people in New Mexico hold the federal Schedule I DEA registration, which is not what the rule requires.

New language added to the rule. Alongside keeping the number, the department added language for how the certifying clinician evaluates a patient, with three ways to meet the in-person requirement so it need not fall only on the certifying clinician. This is the current draft language as of July 17, 2026:

Current draft language · certifying clinician · July 17, 2026

(c) The certifying clinician has evaluated the medical appropriateness of the patient’s proposed enrollment in the New Mexico psilocybin program, and that, in the clinician’s professional opinion, the potential health benefits of the medical use of psilocybin would likely outweigh health risks for the patient; and

  1. the certifying clinician has conducted an in-person examination of the patient within the previous six months;
  2. the certifying clinician has conducted a patient evaluation via telemedicine and has reviewed the medical records pertaining to the diagnosis of a qualifying condition and has confirmed the medical records of the diagnosis are from a clinician who has conducted an in-person examination of the patient within the previous six months; or
  3. the certifying clinician has conducted a patient evaluation via telemedicine and has had a formal consult with a clinician who has conducted an in-person exam with the patient within the previous six months; and

Source: language the department stated at the July 17, 2026 Advisory Board meeting. All three pathways now appear in the July 23 published proposed rule at 7.35.3.8 (B)(8)(c) and 7.35.3.13 (A)(2).

What is still open. The rule is not final. It goes to a public rule hearing on August 28, 2026 before it can take effect; on July 17 the department said only that it was looking at the end of August, and the date was set when the rule was published. Three threads were left unresolved and none of them is answered in the published text:

  • How many New Mexico providers hold prescriptive authority but no controlled-substance number. The board asked the department to check with the Regulatory Licensing Division and Dr. Culpepper.
  • Whether the “risk and benefit” wording in paragraph (c) should be narrowed. In public comment, Denali said requiring a full risk-benefit analysis, rather than an “assessment of medical risk,” raises the clinician’s exposure and the chance of insurance clawbacks on a Schedule I service.
  • Whether federal rescheduling changes the picture. Larry Leeman said a move from Schedule I to Schedule III, which he considers likely by mid-2027, could reopen the requirement through the normal rule-change process.

Chris Peskuski restated his objection: that the requirement is an access bottleneck, that it shifts liability away from the room where the patient is treated, and that it risks “signature mills” without adding safety. The sections below explain what the number is and how this access point compares to other states.

1

What a New Mexico controlled-substance number is

It is a state registration issued by the New Mexico Board of Pharmacy, separate from a federal DEA number. The published rule requires the New Mexico number, not the federal one (7.35.3.9 (D)(2), p. 3).

  • Created by the New Mexico Controlled Substances Act (NMSA 1978, Sections 30-31-1 through 30-31-42) and Board of Pharmacy rule 16.19.20 NMAC.
  • Issued by the New Mexico Board of Pharmacy, within the Regulation and Licensing Department.
  • Who may hold it: only enumerated prescribing and administering license types. The Act’s definition (Section 30-31-2(P)) lists physician, doctor of oriental medicine, dentist, physician assistant, certified nurse practitioner, clinical nurse specialist, certified nurse-midwife, prescribing psychologist, veterinarian, pharmacist and pharmacist clinician, and others “licensed or certified to prescribe and administer drugs.”
  • What it authorizes: to administer, prescribe, or dispense controlled substances in New Mexico, within a “valid practitioner-patient relationship” as defined by the holder’s own licensing board.
  • Versus a DEA number: separate registrations, and the order between them is in dispute. Board of Pharmacy rule 16.19.20.14(B) NMAC lists a current DEA registration among the application materials, while the practice described on the record is that the state number comes first and the DEA number follows. A board member said on July 17, in a transcript that carries no speaker labels: “there are people that have the state controlled substance that don’t have any DEA license.” The department said it is checking the point with the Board of Pharmacy. Both registrations precede enrollment in the state Prescription Monitoring Program.

Sources: 16.19.20 NMAC; NMSA 30-31-2; New Mexico Board of Pharmacy practitioner application; July 17 board transcript, unofficial and not speaker-attributed. The relationship between the state number and a DEA registration is the one point in this section that is not settled; the rest is confirmed against the primary source.

2

Who can diagnose the qualifying conditions, and who needs the number

Under New Mexico law, diagnosis and prescribing authority are separate. A licensed clinical social worker or a licensed psychologist can diagnose PTSD and depression without holding any controlled-substance number.

Social workers. The Social Work Practice Act (Section 61-31-6) defines clinical social work practice to include “the diagnosis, treatment and prevention of psychosocial dysfunction, disability or impairment, including but not limited to emotional and mental disorders,” and defines clinical social work services as “assessment, diagnosis and treatment, including psychotherapy and counseling.” The section says nothing about a controlled-substance registration or prescribing authority. LCSWs have no prescriptive authority in New Mexico.

Psychologists. An ordinary licensed psychologist may diagnose and treat mental disorders but cannot prescribe. New Mexico separately created a “prescribing psychologist” designation and a “conditional prescription certificate”; that subset may “administer and prescribe psychotropic medication” and “must comply with all other state and federal laws regulating the administering and prescribing of controlled substances.” A psychologist without that certificate can diagnose but cannot hold a controlled-substance number as a prescriber.

The effect. Diagnosing a qualifying condition sits within the scope of several non-prescribing license types; holding a controlled-substance number is limited to the prescribing license types in section 1. So the requirement narrows the certifying pool from “those who can diagnose the condition” to “the subset who can also prescribe controlled substances.” The department settled this for the published rule: it declined to accept a non-prescribing provider as a certifying clinician, and 7.35.3.9 (D)(2) requires the number of every applicant for that role. The rule is proposed, not final, and the question can be raised again at the August 28 hearing.

Verified. Sources: NMSA 61-31-6; NMSA 61-9-17.2.

3

What the Medical Psilocybin Act requires

Entry is not based on a diagnosis alone. The Act sets a two-part test: a diagnosed qualifying condition and a separate clinician judgment of medical appropriateness. Its definition of “clinician” names no license type and requires no controlled-substance number.

The program was created by Senate Bill 219, the Medical Psilocybin Act, signed April 2025 and effective June 20, 2025. Its qualifying conditions are major treatment-resistant depression, post-traumatic stress disorder, substance use disorders, end-of-life care, and other conditions the department approves.

“qualified patient” means a patient whose clinician has judged the patient to be a medically appropriate candidate for the use of medical psilocybin based on being diagnosed with a qualifying condition.SB 219, Section 3. The verb “has judged,” with “medically appropriate candidate,” denotes a clinical judgment layered on top of the diagnosis; diagnosis is necessary but not sufficient.
“clinician” means an approved health care provider licensed in New Mexico who holds a permit from the department to provide medical services to qualified patients.SB 219, Section 3. No controlled-substance number and no specific license type appears. Clinician qualifications are delegated to department rulemaking, where proposed rule 7.35.3 and the term “certifying clinician” live.

Scheduling. SB 219 did not move psilocybin to a lower schedule. It kept psilocybin and psilocin in Schedule I and added a medical-use carve-out: each entry now reads “except as provided otherwise in the Controlled Substances Act and the Medical Psilocybin Act,” and a new subsection provides that “the enumeration of psilocybin and psilocin in this schedule does not apply to their medical use as provided in the Medical Psilocybin Act.” The enacted title states the amendment is to “remove psilocybin and psilocin from the schedule for purposes of qualified medical treatment.”

Confirmed against the enacted text. Source: SB 219, Section 30-31-6 amendment.

4

What the number does, and does not do, at this access point

New Mexico’s registration requirement turns on the act a person performs, not on a drug’s schedule number.

A person who manufactures, distributes or dispenses a controlled substance or who proposes to engage in the manufacture, distribution or dispensing of a controlled substance shall obtain a registration issued by the board in accordance with its regulations.NMSA 1978, Section 30-31-12(A). “The board” is the Board of Pharmacy. The trigger is the regulated act, not the schedule number.

Two facts set the frame. First, SB 219 uses “administering” and “recommending,” never “prescribe,” for psilocybin: it protects a clinician “administering… psilocybin” and one “recommending the program.” Second, psilocybin remains a Schedule I substance under federal law, which cannot be prescribed at all (21 U.S.C. Section 829), and an ordinary DEA registration cannot authorize handling it. A certifying clinician who holds a controlled-substance number holds it for their other practice; the number is not, and cannot be, exercised on the psilocybin.

The department’s stated reason and the statutory structure both belong on the record:

  • The department’s stated purpose (July 9): licenses can diagnose some conditions (“a social worker can diagnose… PTSD and depression”), “but the main reason for the controlled substance number is because it is a treatment that is occurring with a medication… that is part of what ensures that there is that medical evaluation, that medical certification.”
  • The structural reading: under Section 30-31-12, registration attaches to manufacturing, distributing, or dispensing, none of which the certifying clinician does to the psilocybin. So the number operates as a credential (a marker of prescriber-grade licensure), not as an authorization used on the drug. New Mexico’s medical-cannabis program has the same shape: providers “certify” or “recommend” rather than prescribe cannabis, and no controlled-substance number is used on the cannabis, because cannabis is federal Schedule I.

On July 9 the board sent this question back to the department to weigh alternatives. The department answered on July 17 that the requirement would stay, and the rule published on July 23 keeps it. Nothing in the published text changes the structural reading above: the number is still not exercised on the psilocybin.

Sources: NMSA 30-31-12; SB 219 Sections 3 and 5; 21 U.S.C. 829; July 9 transcript.

5

How other jurisdictions set the same access point

None of the three comparators gates access through a clinician who holds prescribing authority. Oregon and Colorado require no diagnosis or qualifying condition; Washington, D.C. medical cannabis lets adults self-certify. New Mexico’s proposed rule is the only one of the four that requires a clinician determination for entry.

Oregon (Measure 109 / ORS 475A). The Oregon Health Authority states: “To access psilocybin services, an individual must be 21 years of age or older” and “A prescription or medical referral is not required.” Safety contraindications can disqualify a client during preparation, but that is a disqualifier, not an affirmative diagnosis requirement.

Colorado (Proposition 122 / SB23-290). The implementing law contains no diagnosis, qualifying-condition, or physician-gatekeeper requirement; access is gated by age (21 and older), and the model runs through licensed facilitators and healing centers, not a prescriber. This finding rests partly on the law’s silence, corroborated by secondary legal analysis; rated medium confidence.

Washington, D.C. (medical cannabis). D.C. Code Section 7-1671.05 and D.C. Law 24-187 let adults 21 and older “self-certify… on a form provided by [the regulator] that they are utilizing cannabis for medical purposes,” replacing the prior requirement of a signed practitioner recommendation. Minors still require a recommendation; the permanent authority is D.C. Law 24-332 and the agency is now ABCA.

Verified. Sources: oregon.gov OHA; leg.colorado.gov SB23-290; code.dccouncil.gov.

6

Consultation and telemedicine precedents

Two alternatives were floated July 9: a consultation model and a behavioral-health-plus-telemedicine referral. The published rule took up part of this. 7.35.3.13 (A)(2), p. 8 lets a certifying clinician certify on a telemedicine evaluation, either against a six-month in-person lookback of their own, against records from a clinician who examined the patient in that window, or after a formal consult with that clinician. It did not take up a referral by a non-prescribing behavioral-health provider. The federal precedents below predate the rule and concern prescribing, which differs from certifying a patient for entry; they are context for how the same problem has been handled elsewhere, not endorsements.

  • Covering-practitioner exception. The Ryan Haight Act generally requires one in-person evaluation before remotely prescribing a controlled substance, but permits a practitioner to evaluate a patient by telemedicine “at the request of a practitioner who… has conducted at least 1 in-person medical evaluation of the patient… within the previous 24 months.” It also exempts federal systems (Indian Health Service, Department of Veterans Affairs).
  • Current flexibility. The DEA and HHS extended COVID-era flexibilities a fourth time, effective through December 31, 2026, five months after this page was last checked, letting a DEA-registered practitioner prescribe Schedule II–V controlled substances via telemedicine “without having conducted an in-person medical evaluation,” provided the prescription is for a legitimate medical purpose in the usual course of practice.
  • Proposed permanent rule. The DEA has proposed a “special registration” that would let a patient receive prescribed controlled medications through telemedicine “without ever having an in-person medical evaluation,” covering Schedule III–V, with a narrower Schedule II track for specified board-certified specialties. Proposed, not final.

Extracted from primary sources; not put through the same fact-check as sections 1–5. Sources: APA Ryan Haight toolkit; Federal Register fourth extension; DEA rulemaking.

7

Liability for certifying a patient one will not treat

Board members raised liability for certifying a patient one will not treat on July 9. The general framework: a clinician’s formal decision that a patient foreseeably relies on can create a duty even without hands-on treatment, while informal advice is treated differently. The controlling illustrations are out-of-state case law, used here only to describe the framework, not as New Mexico authority.

The general rule: “Generally, a physician owes no duty to a patient without a physician-patient relationship. Without a physician-patient relationship, with no duty owed, there is no liability for ‘breach’ of that nonexistent duty.”

The exception that applies here: in Warren v. Dinter (Minnesota), the court held that “a duty arises between a physician and an identified third party when the physician provides medical advice and it is foreseeable that the third party will rely on that advice.” A physician who never examined the patient faced liability for a decision the patient relied on. The court distinguished a “formal medical decision” from informal “curbside” advice.

This describes why a certifying-clinician role can carry liability exposure. It does not quantify New Mexico exposure, and no New Mexico certifying-clinician liability authority was located. Whether a psilocybin certification is a “formal medical decision” of the kind that attaches a duty is an unlitigated question.

Illustrative, out-of-state and secondary. Sources: National Legal Research Group; Medical Economics on Warren v. Dinter (Minnesota).

8

New Mexico rural access and prescriber supply

The prescriber-eligible clinicians are the scarcest category and the most concentrated outside rural counties. The non-prescribing clinicians who can diagnose the qualifying conditions are far more available rurally.

  • 27 of New Mexico’s 33 counties are designated, in whole or in part, as health professional shortage areas; almost all counties are a shortage area for mental health.
  • Ten frontier counties, with 27,000 Medicaid managed-care enrollees combined, have no behavioral-health prescribers at all. Nineteen of the 33 counties have fewer than two licensed behavioral-health providers per 1,000 enrollees, all rural or frontier.
  • Rural New Mexico had 40 psychiatrists (5.6 per 100,000) against 306 (21.6 per 100,000) in urban counties; multiple rural counties had zero. Rural social workers, who can diagnose but not prescribe, numbered 997 (140.0 per 100,000), about 25 times the rural psychiatrist rate.
  • Only 29 percent of licensed behavioral-health providers are in rural and frontier counties, where nearly half of Medicaid managed-care enrollees live.

Extracted; not put through the same fact-check as sections 1–5. Sources: HHS OIG OEI-02-17-00490; University of Washington Rural Health Research Center (June 2025); Commonwealth Fund via NM In Depth.

The record

The July 9 discussion, verbatim by speaker

The board did not endorse the requirement and sent it back to the department. No vote was taken. Ian Dunn will take it back to the department to reconsider.

Positions stated on the certifying clinician and the controlled-substance number unofficial July 9 transcript

Department presentation · Dominic Zurlo and reader

“Licenses have the ability to be able to diagnose some of the conditions. And yes, that is true. For example, a social worker can diagnose with regard to PTSD and depression, for example. But the main reason for the controlled substance number is because it is a treatment that is occurring with a medication… with it being a medical program, that is part of what ensures that there is that medical evaluation, that medical certification.”

Chris Peskuski · board member

“I’m concerned that putting the access point through a doctor is going to make it very risky for clinicians to certify anybody into this program because they’re going to be subject to malpractice. I believe all the liability should lie in the room where the patient’s being treated… Why would a clinician sign off on a patient when he’s not gonna be necessarily in the room when all of that happens? My wife hasn’t been able to get a primary care practitioner for over a year now and we live in Albuquerque… The access outside of Bernalillo County is going to be unattainable. I would recommend that we look towards a model of consultation… where the practitioners are required to consult… to determine medical readiness… and allows for continuity of care for practitioners to work with doctors that are already treating patients. And I think it solves a lot of these issues of liability and accessibility.”

Dan Jennings · board member

“From rural area, my big concern… is that I would have to find this person who is a doctor, who has a CS, who has gone through the program, and I physically have to travel to them… it won’t be here. And I could not do it via tele. The only time I could is if I get recertified… if you’re a patient that is an end-of-life, that means that end-of-life patient must go to that physician… if my mom who died of cancer would need to get this, she would physically not be able to be in this program.”

Ian Dunn · chair

“One of the models I was comparing it to was the Washington DC medical cannabis model which allows you to self-certify. So what if we could provide them with a list of contraindications, say, ‘Hey, you got any of this?’ If they say no, then we can move them on… existential distress associated with a life limiting illness… That’s not in the DSM-5. That doesn’t need to be vetted by someone with diagnostic authority. I could self-certify.”

Brenda Burgard · board member

“This whole week was me trying to find doctors and psychiatrists for my patients currently. For example, for Adderall, the hoops that people have to jump through just to get the medical clearance and then try to find a psychiatrist to prescribe because doctors don’t want to prescribe Adderall… we’re looking at anywhere between three and six months of this type of bottleneck. As Ian said, this is the real world and I think that we really need to think all of this again.”

Keenan Ryan · Acting CMO, Medicaid (covering designee)

“Is it possible to [allow] all behavioral health providers and allow through telemedicine? Would that be a meaningful compromise, to allow some sort of recommendation or referral without being restrictive? Some therapists may not have a controlled substance because they’re not prescribing, or they might be a psychologist without it, but they could still say that you have PTSD, for example, that would be within their scope and could refer. So just throwing out some options along this spectrum between complete in-person controlled substance versus all self-certified. I think there could be a happy medium in there.”

Outcome · Dominic Zurlo

“What’s the final action on the certifying clinician? So Ian will take that back to here in the department to reconsider.”