A legal guide for practitioners, policymakers, and telemedicine companies.

On February 24, 2023, the Drug Enforcement Agency announced proposed rules for prescribing controlled substances via telemedicine after the COVID-19 Public Health Emergency expires. The proposed rules are open for public comment for only thirty days, after which DEA will issue final regulations. 

The proposed rules are intended to bridge between the DEA’s current PHE waivers and a post-PHE environment. In so doing, DEA proposed creating two new limited options for telemedicine prescribing of controlled substances without a prior in-person exam. The options both complex and more restrictive than what has been allowed for the past three years under the PHE waivers.  The DEA’s proposal will discontinue the ability for telemedicine prescribing of controlled substances where the patient never has any in-person exam (with the exception of an initial prescription period of no more than 30 days’ supply).  Moreover, if the patient requires a Schedule II medication or a Schedule III-V narcotic medication (with the sole exception of buprenorphine for opioid use disorder (OUD) treatment), an initial in-person exam is required before any prescription can be issued.

Unquestionably, the DEA’s proposal is not what most industry stakeholders were anticipating. The initial reaction is the rules are more restrictive than necessary and impose concerning limitations and burdens on clinicians and the patients they treat.

Buprenorphine.  Even more alarming are risks the proposed rules could harm patients seeking or already receiving buprenorphine for treatment of OUD. DEA’s companion proposed rule on buprenorphine can be found here.  For the last year, there have been repeated assurances by HHS, DEA, SAMHSA, ONDCP, and the White House that these buprenorphine patients will not fall off the Telehealth Cliff.  Yet, the DEA’s rule will require these patients to have in-person exams and block them from fully-virtual telemedicine care. This includes those patients who are currently taking buprenorphine for medication assisted treatment (MAT) and who have not had a prior in-person exam.  (Keep in mind: buprenorphine is a partial opioid agonist, unlike methadone or morphine, and reported as less likely to be abused or diverted.)  Unless the proposed rule is changed, stakeholders are left to ask: Will DEA’s decision to end telemedicine-only buprenorphine help, or will it harm patients struggling with opioid use disorder and trigger more overdoses and diversion?

Special Registration for Telemedicine. In another disappointing turn, the proposed rules fail to include the long-awaited telemedicine special registration regulation, designed to allow certain clinicians the ability to prescribe controlled substances via telemedicine without conducting an in-person exam of the patient. 

This guide: 1) summarizes the key elements and requirements contained in the proposed rule; 2) explains how it differs from the special telemedicine registration rule; and 3) describes what stakeholders can do to make their voice heard, including by submitting comments to the proposed rule, during these next 30 days.

Key Provisions Under the DEA’s Proposed Rule

1. What is the Ryan Haight Act?

The statutory basis for the proposed rule is the Ryan Haight Online Pharmacy Consumer Protection Act of 2008 (Ryan Haight Act), which prohibits the distributing, dispensing or delivery of controlled substances via the Internet without a valid prescription.  It applies only in limited circumstances where the practitioner wishes to prescribe a controlled substance via telemedicine and has never conducted an in-person medical exam of the patient.

The Ryan Haight Act requires a practitioner to conduct at least one in-person medical evaluation of the patient before prescribing a controlled substance by means of the “Internet” (a broadly-defined term that includes telemedicine).  Once the practitioner has conducted this in-person medical evaluation, the Ryan Haight Act does not set an expiration period or a minimum requirement for subsequent annual exams.  Failure to conduct this in-person medical evaluation can constitute a per se violation of the Controlled Substances Act and result in civil and criminal penalties.

The Ryan Haight Act was designed to combat the proliferation of so-called “rogue Internet sites” that unlawfully dispensed controlled substances by means of the Internet, including online pharmacies offering controlled substances without a valid doctor-patient relationship.  Yet the broad language of the Ryan Haight Act applies not only to pharmacies, but also to legitimate practitioners who prescribe controlled substances via telemedicine. 

In the years since it was enacted, the DEA has used the Ryan Haight Act to regulate the marketplace, sanctioning practitioners and pharmacies whose unethical and substandard prescribing practices violated the law.

2. Is the proposed rule one of the “practice of telemedicine” exceptions under the Ryan Haight Act?

Yes.  The Ryan Haight Act contains seven “practice of telemedicine” exceptions to the in-person medical evaluation requirement. These are seven distinct categories Congress determined were appropriate to allow for telemedicine prescribing of controlled substances despite the practitioner never having examined the patient in person. Some of the exceptions are suited to institutional/hospital arrangements, but most have limited to no use in contemporary telemedicine services, particularly direct-to-patient care when the patient is located at home. 

The seven exceptions are: 1) treatment in a hospital or clinic; 2) treatment in the physical presence of a DEA-registered practitioner; 3) treatment by Indian Health Service or Tribal practitioners; 4) treatment during a public health emergency as declared by the Secretary of Health and Human Services; 5) treatment by a practitioner who has obtained a “special registration”; 6) treatment by Department of Veterans Affairs practitioners during a medical emergency; and 7) other circumstances specified by regulation. See 21 C.F.R. § 1300.04(i)(1)-(7).

The proposed rule creates a new option under exception #7, a flexible catch-all exception (“The practice of telemedicine is being conducted under any other circumstances that the [DEA] Administrator and the Secretary of Health and Human Services have jointly, by regulation, determined to be consistent with effective controls against diversion and otherwise consistent with the public health and safety.”).  The requirements in the proposed rule apply to “telemedicine prescriptions” under 21 C.F.R. § 1306.31 conducted pursuant to 21 U.S.C. § 802(54)(G). 

3. What is the proposed rule intended to accomplish?

According to the DEA’s statements, the proposed rule is designed to ensure that patients do not experience lapses in care, and to ensure continuity of care under the current telehealth flexibilities in place as a result of the COVID-PHE.

The two new options introduced in the proposed rule are:

1. A virtual first process where a practitioner can issue an initial prescription for a controlled substance without having conducted an in-person exam of the patient, but only if: 1) the medication is a non-narcotic Schedule III, IV, or V controlled substance (or buprenorphine for treatment of OUD); and 2) the prescribed amount does not exceed 30 days. This is called a “telemedicine prescription.” Before any additional prescribing can occur, the patient must undergo an in-person exam.

2. A “qualified telemedicine referral” process where a patient has an initial in-person exam with a practitioner, who subsequently refers the patient to a second practitioner. The second practitioner can have a telemedicine exam of the patient and prescribe a controlled substance without personally conducting an in-person exam of the patient. Under this referral process, the telemedicine practitioner can prescribe Schedule II-V and narcotic controlled substances.

Compared to the original Ryan Haight Act, these new options are expanded flexibilities intended to allow more telemedicine-based care, but are more restrictive than what has been allowed for the past three years under the PHE waivers.  DEA’s proposal will discontinue the ability for telemedicine prescribing of controlled substances where the patient never has any in-person exam (with the exception of an initial prescription period of no more than 30 days’ supply).  Moreover, if the patient requires a Schedule II medication or a Schedule III-V narcotic medication (with the sole exception of buprenorphine for OUD treatment), an initial in-person exam is required before a prescription can be issued.

4. Does the proposed rule apply to any and all telemedicine prescribing of controlled substances under the Ryan Haight Act (e.g., even if a different practice of telemedicine exception is met, or if the practitioner conducted a prior in-person exam)?

No. The requirements in the proposed rule affect what DEA refers as “a narrow subset of telemedicine consultations.” Specifically, practitioners who issue “telemedicine prescriptions” under Section 802(54)(G) – the newly-created option under the proposed rule.  DEA stated “[t]his rulemaking would not impose any new requirements on practitioners authorized to practice telemedicine under other statutory exceptions in 21 U.S.C. § 802(54) […].” According to the DEA’s commentary, press release documents, and highlight summary, the limitations and requirements in the proposed rule do not apply if:

1. The prescribing telemedicine practitioner has conducted at least one in-person exam of the patient before prescribing controlled substances.

2. The prescribing telemedicine practitioner meets one of the other practice of telemedicine exceptions under the Ryan Haight Act.

3. The patient has been referred to the prescribing telemedicine practitioner by another practitioner who previously conducted an in-person exam of the patient. (Although there are certain requirements for the qualified telemedicine referral process itself, which is a newly-proposed process.)

5. What is the proposed definition of “telemedicine prescription”? What effect will this phrase have on practitioners, pharmacies, and patients?

Telemedicine prescription means “a prescription issued pursuant to § 1306.31 by a physician, or a “mid-level practitioner” as defined in 21 § CFR 1300.01(b), engaging in the practice of telemedicine as defined in 21 C.F.R. § 1300.04(j).”  It is a specifically-defined term of art in the proposed rule.

In plain English, the term “telemedicine prescription” refers only to a prescription issued under the new options (virtual first and qualified telemedicine referral) created under the proposed 21 C.F.R. § 1306.31 as authorized by 21 U.S.C. § 802(54)(G).  The term does not apply to prescriptions issued under any of the other six “practice of telemedicine” exceptions under the Ryan Haight Act (21 U.S.C. § 802(54)(A)-(F)).  Nor does it apply to prescriptions where the practitioner conducts an initial in-person exam and then subsequently prescribes via telemedicine or other modalities. “Telemedicine prescription” does not mean any and all controlled substance prescriptions issued from a telemedicine exam. 

This is important to consider because words matter. The term “telemedicine prescription” appears broad to the casual reader, while the actual definition of the term is quite narrow and specific to only the two newly-proposed options.  As a result, this terminology will very likely cause widespread confusion among practitioners, pharmacies, health plans, patients, and the industry because many will mistakenly apply the term to any and all prescriptions issued via telemedicine.  This could trigger significant administrative burden, unnecessary complexity, and ultimately frustration.  The foreseeable result will be fear and reluctance among practitioners to engage in telemedicine post-PHE, leaving patients without access to important, necessary medicines from legitimate practitioners. This includes practitioners who will mistakenly assume that conducting a video visit always means a “telemedicine encounter” or results in a “telemedicine prescription.”  If nothing else, DEA might consider swapping “telemedicine prescription” for a different turn of phrase to better reflect how this is specific only to the newly-proposed options under 21 U.S.C. § 802(54)(G) and does not apply to the majority of controlled substance prescriptions issued via telemedicine.

6. Are patients who received a telemedicine-only exam during the COVID-19 PHE “grandfathered” or must they have an in-person exam before the COVID-19 PHE ends on May 11, 2023?

The Controlled Substances Act does not have a feature allowing patients to be “grandfathered” from the in-person exam requirement at the conclusion of a PHE.  The current DEA waiver of the in-person exam requirement falls under exception #4 of the Ryan Haight Act, i.e., the PHE.  It will expire when the COVID-19 PHE ends May 11, 2023. 

To address this, the proposed rule creates a new term, “telemedicinerelationship established during the COVID-19 public health emergency.” Such a relationship exists if: 1) between March 16, 2020 and May 11, 2023 (i.e., the PHE period); 2) the practitioner prescribed a controlled substance based on a telemedicine encounter; and 3) the practitioner never conducted an in-person exam of the patient.

In that situation, the DEA will extend the in-person exam waiver an additional 180 days, making the new deadline early November 2023 (or later if the final rule publishes after May 11).  For any prescribing after that date, that practitioner must either conduct an in-person exam, meet a different telemedicine exception under the Ryan Haight Act, or stop prescribing for the patient.

Note: this feature does not allow practitioners to use PHE waivers for new patients after May 11, 2023.  Namely, if a practitioner has a telemedicine consult with a new patient on May 12, 2023, neither the old PHE waivers nor this extension will apply.  That’s because this new doctor-patient relationship would not constitute a telemedicine relationship established during the COVID-19 public health emergency.

7. Does the proposed 180-day extension for telemedicine relationships established during the PHE apply to Schedule II controlled substances and other narcotics?

Yes.  According to the DEA’s proposed rule, this allowance “applies to all schedule II-V controlled substances in all areas of the United States.”

8. What is the virtual first “telemedicine prescription” option under the proposed rule? How does this new process work?

Under this proposed process, a practitioner can use telemedicine to issue an initial “telemedicine prescription” for a controlled substance without first conducting an in-person exam of the patient.  This process works even if the practitioner cannot meet any other exception under the Ryan Haight Act or if they did not receive a qualifying telemedicine referral.  The intended use case is for telemedicine-only consults with new patients.

The process works like this:

1. A DEA-registered practitioner conducts a telemedicine exam of a patient whom the practitioner never had any prior in-person exam.

2. The practitioner must review and consider the prescription drug monitoring program (PDMP) database in the state where the patient is located (if the state has a PDMP) for data regarding any controlled substance prescriptions issued to the patient in the last year, or, if less than one year of data is available, in the entire available period.

   1. If the practitioner is unable to obtain the PDMP data due to the PDMP system being non-operational or otherwise inaccessible as a result of a temporary technological or electrical failure, then:

      1. The practitioner may issue the prescription for no more than a 7-day supply;

      2. The practitioner must subsequently obtain the PDMP data and conduct the review within 7 days of the telemedicine encounter; and

      3. The practitioner must record the attempts to obtain the PDMP data.

   2. If the practitioner fails to obtain the required PDMP data, the practitioner must record the dates and times the practitioner attempted to gain access, the reason why the practitioner was unable to gain access, and any follow-up attempts made to gain access to the system.

3. The practitioner can issue an initial prescription, but only for a non-narcotic Schedule III, IV, or V controlled substance (or buprenorphine for treatment of opioid use disorder).

4. The prescription is limited to a maximum 30-day supply.

   1. Technically, the practitioner is allowed to issue multiple prescriptions for the same patient, but only prescribe an amount less than or equal to a total quantity of a 30-day supply. This supply may include dosages that are titrated up or down depending on the patient’s response to the medication and the practitioner’s medical judgment, but may not exceed a supply sufficient to treat the patient for more than 30 days.

5. The practitioner must impose a notation on the face of the prescription, or within the prescription order if prescribed electronically, that the prescription has been issued via a telemedicine encounter.

6. All prescribing is done for a legitimate medical purpose in the usual course of professional practice, and in compliance with applicable state and federal laws.

7. After 30 calendar days from the date the initial telemedicine prescription was issued, the practitioner cannot issue any more telemedicine prescriptions for the patient until one of the following occurs (all of which require some type of in-person exam with the patient).DEA gave three different options to choose from:

   1. The prescribing telemedicine practitioner conducts an in-person exam of the patient.

   2. The patient participated in a 3-party exam (patient, in-person practitioner, and telemedicine practitioner simultaneously) where the patient is being treated by, and in the physical presence of, the in-person DEA-registered practitioner acting in the usual course of professional practice. The telemedicine practitioner participates simultaneously in this exam using interactive audio-video (audio-only is never allowed during this exam, even for telemental health or if audio-only was allowed for the initial consult). Under this option, even though the telemedicine practitioner would never personally conduct any in-person exam of the patient, they may rely on the in-person evaluation conducted by the on-site practitioner – and remotely observe this evaluation via video and audio – when determining whether to continue prescribing to the patient.

   3. The patient goes to a different DEA-registered practitioner for an in-person exam, and that practitioner sends the prescribing telemedicine practitioner a qualifying telemedicine referral for the patient.

If one of the above options is met, the telemedicine practitioner can continue prescribing a controlled substance to the patient without additional in-person exams, so long as doing so was consistent with legitimate medical purposes and a subsequent evaluation is not required by law. If not, the practitioner cannot issue any more telemedicine prescriptions for that patient until one option is met.

9. Why are Schedule II and narcotic controlled substances excluded from the virtual first “telemedicine prescription” process?

As stated in the proposed rule, the DEA “believes that allowing for the prescription of any schedule II substances or the general prescription of narcotic controlled substances as a result of telemedicine encounters would pose too great a risk to the public health and safety.” However, if the prescribing telemedicine practitioner receives a qualifying telemedicine referral for the patient, a prescription may be issued for any controlled substance the practitioner is otherwise authorized to prescribe under applicable laws and regulations, including Schedule II and narcotic controlled substances.

10. What is a “qualifying telemedicine referral” under the proposed rule? How does this new referral-based process work?

A qualifying telemedicine referral means “a referral to a practitioner that is predicated on a medical relationship that exists between a referring practitioner and a patient where the referring practitioner has conducted at least one medical evaluation in the physical presence of the patient, without regard to whether portions of the evaluation are conducted by other practitioners, and has made the referral for a legitimate medical purpose in the ordinary course of their professional practice. A qualifying telemedicine referral must note the name and National Provider Identifier (NPI) of the practitioner to whom the patient is being referred.”

In plain English, a qualifying telemedicine referral process would work as follows:

1. A DEA-registered practitioner conducts at least one in-person exam of the patient in accordance with applicable state law.

2. That practitioner refers the patient to a second practitioner for a legitimate medical purpose in the ordinary course of their professional practice. The practitioner must make a written referral (containing specific content) and send it to the second practitioner.

3. The second practitioner conducts a telemedicine exam of the patient. This telemedicine exam need not occur simultaneously with the first in-person exam. The second practitioner need not conduct an in-person exam.

4. The second practitioner must review and consider the PDMP database in the state where the patient is located (if the state has a PDMP) for data regarding any controlled substance prescriptions issued to the patient in the last year, or, if less than one year of data is available, in the entire available period.

   1. If the practitioner is unable to obtain the PDMP data due to the PDMP system being non-operational or otherwise inaccessible as a result of a temporary technological or electrical failure, then:

      1. The practitioner may issue the prescription for no more than a 7-day supply;

      2. The practitioner must obtain the PDMP data and conduct the review within 7 days of the telemedicine encounter; and

      3. The practitioner must record the attempts to obtain the PDMP data.

   2. If the practitioner fails to obtain the required PDMP data, the practitioner must record the dates and times the practitioner attempted to gain access, the reason why the practitioner was unable to gain access, and any follow-up attempts made to gain access to the system.

5. The second practitioner can prescribe a controlled substance, including Schedule II and narcotic controlled substances.

6. The practitioner must impose a notation on the face of the prescription, or within the prescription order if prescribed electronically, that the prescription has been issued via a telemedicine encounter.

There is no requirement for the patient to undergo a subsequent in-person exam by either the first or second practitioner, nor must the patient obtain subsequent referrals in order for the telemedicine practitioner to prescribe again in the future.  Of course, if an in-person exam is required by state law, other applicable federal law, or standards of clinical practice, such in-person exam must be conducted.

If, for some reason, multiple DEA-registered practitioners were physically present during the patient’s in-person exam, each of those practitioners would have the ability to issue a qualifying telemedicine referral.  Referrals predicated exclusively on a telemedicine exam do not constitute a qualifying telemedicine referral.

The qualifying referral process requires special documentation and timing. The written referral must be based on the diagnosis, evaluation, or treatment that occurred as a result of the in-person medical evaluation. Along with the written referral form, the referring practitioner must communicate the results of the in-person evaluation by sharing the relevant information in the patient’s medical record which includes, at a minimum, the diagnosis, evaluation, and treatment of the patient. All of this must occur and be received by the second practitioner before a prescription is issued by the second practitioner.

The written referral form must also include: 1) the name and NPI of the referring practitioner (i.e. the one who conducted the in-person exam) and 2) the name and NPI of the telemedicine practitioner (i.e., to whom the patient is being referred).  This means the referring practitioner cannot simply refer a patient to a business entity, medical group, facility, or specialist practice, but instead must name a specific practitioner on the referral form.

Both the referring practitioner and the receiving practitioner must maintain copies of all qualifying telemedicine referrals they issue or receive.

11. Are Schedule II and narcotic controlled substances allowed under the “qualifying telemedicine referral” process in the proposed rule?

Yes. According to the DEA, if the qualifying telemedicine referral requirements are met, the prescription issued may be for any controlled medication the telemedicine practitioner is otherwise authorized to prescribe under applicable laws and regulations.

12. Who can serve as the referring practitioner who conducts the initial in-person exam of the patient?

The referring practitioner must be DEA-registered practitioner acting in the usual course of professional practice.

13. Are there any new recordkeeping requirements contained in the proposed rule?

Yes, there are many specific recordkeeping requirements, some of which will be burdensome on practitioners and patients, particularly as the proposed referral documentation is more onerous and complicated than how practitioners currently make referrals for patients. Practitioners must keep detailed records of the “telemedicine prescriptions” they issue and all “qualifying telemedicine referrals” they send or receive. 

For each “telemedicine prescription,” the prescribing practitioner must maintain a written or electronic record indicating:

1. The date the prescription was issued;

2. The full name and address of the patient;

3. The drug name, strength, dosage form, quantity prescribed, and directions for use;

4. The address at which the practitioner, and the city and State in which the patient, are located during the telemedicine encounter;

5. If the telemedicine prescription was issued through a qualifying telemedicine referral:

   1. The name and NPI of the referring practitioner;

   2. A copy of the referral document and other communications from the referring practitioner (e.g., the results of the evaluation by sharing the relevant information in the patient’s medical record which includes, at a minimum, the diagnosis, evaluation, and treatment of the patient); and

6. All efforts to comply to access the PDMP system.

The following additional records must be maintained when using the 3-party exam option under the virtual first “telemedicine prescription” process:

1. The local in-person practitioner physically present with the patient must maintain, for each such medical evaluation:

   1. The date and time of the evaluation;

   2. The address at which the in-person practitioner is physically present with the patient during the exam;

   3. The address at which the prescribing telemedicine practitioner is located during the telemedicine encounter; and

   4. The NPI of the prescribing telemedicine practitioner.

2. The prescribing telemedicine practitioner must maintain, for each such medical evaluation:

   1. The date and time of the evaluation;

   2. The address at which the prescribing telemedicine practitioner is located during the telemedicine encounter;

   3. The address at which the in-person practitioner is physically present with the patient during the exam; and

   4. The NPI of the in-person practitioner physically present with the patient.

According to DEA’s commentary in the proposed rule, these new recordkeeping requirements only apply “telemedicine prescriptions” via Ryan Haight Act exception #7 (21 USC 802(54)(G)).  Practitioners who rely on any of the other six “practice of telemedicine” exceptions under the Ryan Haight Act (21 U.S.C. 802(54)(A)-(F)), are not subject to these additional recordkeeping requirements because those prescriptions do not fall within the definition of “telemedicine prescription.”  The same goes for a practitioner who conducts an in-person exam of the patient and later uses telemedicine technologies for subsequent prescribing.  (Under the standard federal rule at 21 CFR 1304(c), a DEA-registered individual practitioner is not required to keep records of controlled substances in Schedules II, III, IV, and V that are prescribed in the lawful course of professional practice, unless such substances are prescribed in the course of maintenance or detoxification treatment of an individual.)

14. Where must these special records be maintained and stored?

The records must be maintained at the practitioner’s registered location. This would be the place listed on the certificate of registration issued pursuant to section 303(f) of the Act (21 U.S.C. § 823(g)) (i.e., the practitioner’s 21 C.F.R. § 1301.13(e)(1)(iv) registration).  The records must be in digital or paper form that is readily accessible.

If the practitioner holds more than one registration location, the practitioner must designate one location and maintain all such records at that location. The DEA’s proposed rule recognizes how “a practitioner using telemedicine may operate out of multiple locations” and DEA investigators therefore want the ability to easily obtain all records from a single or centralized location. 

If the practitioner is exempt from registration, the practitioner must maintain these telemedicine records at the location where they maintain other records related to controlled substances.

These special recordkeeping rules, DEA contends, would “serve to reinforce the obligation of practitioners who practice telemedicine to prescribe within the limited circumstances set forth in the proposed rule.”  Ensuring ready access to these records in a consolidated manner in a central location during investigations facilitates DEA’s ability to detect patterns of potential illegitimate prescribing and thus enhance its ability to prevent further diversion of controlled medications.

15. Are there any special notations to make on the prescription itself required by the proposed rule?

Yes.  All “telemedicine prescriptions” issued pursuant to a telemedicine encounter must include a notation on the face of the prescription, or within the prescription order if prescribed electronically, that the prescription has been issued via a telemedicine encounter.  This will be a flag to all pharmacies that the prescription was from a telemedicine consult. It could result in pharmacies electing not to fill otherwise valid prescriptions, simply because the consult was conducted via telemedicine. Indeed, news reports reveal these denials are already occurring. This probability is particularly troubling due to the likelihood practitioners will misinterpret the term “telemedicine prescription” and assume it applies to all prescriptions issued via telemedicine. The DEA’s proposed use of the term “telemedicine prescription” could become a stigma. 

16. What telemedicine modality is required before a controlled substance can be prescribed without an in-person exam?

In short, an interactive audio-video telecommunications system.  The proposed rule revises the modality definition to mirror the Medicare definition under 42 C.F.R. § 410.78(a)(3). This is not a substantive change to Ryan Haight Act requirements, with the exception of treatments for a mental health disorder (discussed further below).

17. Under the proposed rule, can a practitioner use audio-only (instead of interactive audio-video) when prescribing controlled substances to patients for treatment of a mental health disorder?

Yes, it is possible but the use case is limited and situational. Under most circumstances, a telemedicine practitioner must use interactive audio-video. But because the proposed rule now incorporates by reference the Medicare definition of telehealth modality, it also incorporates the recent Medicare changes for audio-only telemental health services while the patient is located at home.

In the proposed rule, DEA set forth four requirements before audio-only equipment is allowed:

1. The telemedicine service at issue must be furnished for purposes of diagnosis, evaluation, or treatment of a mental health disorder.

2. The service must be provided to a patient located in their home. Home includes temporary lodging such as hotels and homeless shelters as well as locations a short distance from the patient’s home (e.g., if the patient, for privacy or other personal reasons, chooses to travel a short distance ways from the exact home location during a telehealth service).

3. The telemedicine practitioner must be technically capable of meeting the audio-video interactive communication standard. This means the telemedicine practitioner must have audio-video equipment at the ready and must make that option available to the patient.

4. The patient is not capable of, or does not consent to, the use of video technology. This means the audio-only option may only be used if the patient is unable to use, does not wish to use, or does not have access to two-way, audio/video technology.

If the telemedicine practitioner meets all the various requirements under the Medicare regulation (42 C.F.R. § 410.78(a)(3)) to use audio-only equipment for telemental health, that practitioner may conduct a telemedicine encounter and prescribe a controlled substance to the patient without using interactive audio-video.  These requirements should be documented in the patient’s record.  Of course, the practitioner must meet all the other requirements of the rule as well as relevant state and federal laws.

18. How does the proposed rule work with state laws? If a state law allows telemedicine prescribing of controlled substances without an in-person exam, does the more permissive state law preempt the Ryan Haight Act?

No.  The Ryan Haight Act preempts state law on telemedicine prescribing of controlled substances, but only to the extent the federal provisions are more restrictive/stringent than the state law.  If the federal Ryan Haight Act is more restrictive than the state law, the more restrictive federal provisions apply. If the state law is more restrictive than the federal Ryan Haight Act, the more restrictive state law provisions apply.  Therefore, the prescribing practitioner must comply with both state and federal laws, and can do so by following the most restrictive provisions under each. 

As a general matter, the federal Ryan Haight Act in-person exam requirement is more stringent than most state laws or state telemedicine requirements. In some states, an in-person examination is not a prerequisite to prescribe controlled substances.  Instead, the state law permits a practitioner to treat a patient through telemedicine, provided the practitioner creates a valid doctor-patient relationship, conducts a sufficient examination of the patient via telemedicine, and meets other state requirements.

19. Can a practitioner issue a “telemedicine prescription” when the practitioner is located outside the United States?

No.  Under the proposed rule, a practitioner who wishes to issue a “telemedicine prescription” must be located in a State, Territory, or possession of the United States; the District of Columbia; or the Commonwealth of Puerto Rico at the time or the telemedicine encounter. Note: this geographic restriction applies to the new options for “telemedicine prescriptions” under 21 C.F.R. § 1306.31 conducted pursuant to 21 U.S.C. § 802(54)(G). 

20. Does the proposed rule alter current DEA controlled substance practice location registration requirements?

Yes.  Under the proposed rule, if a practitioner wishes to issue a “telemedicine prescription,” they must have a DEA registration in both the state where the patient is located and the state where the practitioner is located (i.e., even if the practitioner does not prescribe to patients located in that state, such as a vacation home). Note: this registration requirement applies to the new options for “telemedicine prescriptions” under 21 C.F.R. § 1306.31 conducted pursuant to 21 U.S.C. § 802(54)(G). 

However, outside the “telemedicine prescription” option, the proposed rule makes no mention of the current COVID-19 PHE waivers on DEA state-by-state practice location registrations. The proposed rule does not explain what DEA will do with that waiver come May 11, 2023. Will the DEA will also apply a 180 day extension to its state-by-state registration requirements?  And if so, does DEA have a proposal for practice location registration applications when the practitioner has a multistate telemedicine practice? This is an area that deserves clarification in the responses to comments in the final rule.

21. What about buprenorphine patients receiving treatment for Opioid Use Disorder?

On February 24, 2023, the DEA also announced a Notice of Proposed Rulemaking on “Expansion of induction of buprenorphine via telemedicine encounter.”  That rule, a companion to this proposed rule, is available.  It would expand the circumstances under which the induction of buprenorphine can occur for maintenance treatment and detoxification treatment OUD via telemedicine.  Although the content of that proposed rule is not summarized in this guide, there is much overlap between the two proposed rules.  So much so that DEA is seeking comments on whether it should combine the two Notices of Proposed Rulemaking when publishing the final rule, as both documents refer to prescribing via telemedicine pursuant to 21 U.S.C. § 802(54)(G).

22. What about practitioners employed by the Department of Veterans Affairs?

There are additional rules and requirements for practitioners employed by the Department of Veterans Affairs, who must comply with an additional administrative requirement. Before issuing a “telemedicine prescription,” such practitioners must review not only 1) the state PDMP but also 2) the Department of Veterans Affairs internal prescription database.

23. Is this proposed rule the same as the long-awaited telemedicine special registration rule?

No, it is not.  The proposed rule is definitively and categorically not the same as the special registration rule.  The special registration is exception #5 under the Ryan Haight Act (21 U.S.C. § 802(54)(E)) (“The practice of telemedicine is being conducted by a practitioner who has obtained from the [DEA] Administrator a special registration”). The proposed rule is exception #7 under the Ryan Haight Act (21 U.S.C. § 802(54)(G)). The two exceptions reflect different statutory sections and authority, different processes, and serve to fulfill different, although overlapping, public policy goals. 

The telemedicine special registration is important because it can more readily allow for legitimate direct-to-patient services when the patient is located outside a hospital facility (e.g., at home).  The registration is for practitioners willing to go an extra level further, completing an second application and undergoing (presumably) a more extensive and specialized application than what is required for standard DEA registration.  And the special registration process itself is the medium for DEA to realize the centralized recordkeeping, prescription tracking, and data monitoring tools it requests to police prescribing practices while not saddling patients with an arbitrary in-person exam.

The special registration statutory exception has been around since 2008, but the DEA has never published a rule allowing clinicians to use it.  For nearly 14 years, patients, clinicians, industry stakeholders, and federal elected officials have asked the DEA to activate the special registration. 

Moreover, DEA has been mandated, by both the Legislative and Executive Branches of the United States government, to publish final regulations activating the special registration.  The statutory requirement is contained in the SUPPORT Act, and the DEA was required to promulgate such regulations by October 24, 2019.  Nonetheless, no rule has been published.

In the proposed rule, DEA explained its reasoning why it chose not to publish the special registration rule.  It said:

DEA considered allowing the practice of telemedicine pursuant to an application and issuance of a “special registration” allowing such practice. Upon further consideration, this alternative was deemed potentially burdensome for both prospective telemedicine providers and patients. Therefore, DEA decided against this alternative.

In other words, despite the history of the Ryan Haight Act, 14 years of advocacy efforts and calls for action, and a 2018 federal law mandating DEA publish the special registration, DEA decided not to do so on the grounds it “was deemed potentially burdensome for both prospective telemedicine providers and patients.” Instead, DEA proposed a rule with a complex architecture of different and new exceptions, confusing terminology, and extensive administrative recordkeeping.

Even more, DEA now claims its current proposed rule satisfies its duty to promulgate the special registration.  DEA wrote:

In the SUPPORT for Patients and Communities Act (SUPPORT Act), signed into law on October 24, 2018, Congress required DEA to promulgate regulations concerning such special registrations. See id. 831(h)(2). This instance of rulemaking [i.e., the DEA’s February 2023 proposed rule], which sets forth circumstances under which telemedicine encounters may result in the prescription of controlled substances without an in-person evaluation and also provides safeguards for such prescriptions, is consistent with, and fulfills, DEA’s obligations under both the Ryan Haight Act and the SUPPORT Act.

The DEA contends it has somehow fulfilled its legal obligation to publish the special registration rule, despite never actually publishing the special registration rule.  The DEA provided no legal basis or analysis for its assertion. 

Make Your Voice Heard: How to Submit Comments to the DEA

DEA is soliciting comments until 11:59 p.m. on March 28, 2023. Anyone may submit comments – anonymously or otherwise – via electronic submission. When commenting, refer to “Docket No. DEA-407” on all correspondence, including attachments. Alternatively, commenters may submit comments by mail to:

• Drug Enforcement Administration, Attn: DEA Federal Register Representative/DPW, 8701 Morrissette Drive, Springfield, VA 22152.

Potential areas for comment include, but are not limited to:

• Why is there no telemedicine-only option for patients receiving buprenorphine for OUD treatment? Is that fair? Is that safe? Will requiring an in-person exam for this specific subset of patients limit access to necessary treatment and cause more harm than good?

• DEA claims these new changes do not affect current telemedicine consults. Can it confirm the actual changes in the regulations and new definitions will not more broadly affect telemedicine prescribing of controlled substances, if done outside of the newly-proposed option under 21 U.S.C. § 802(54)(G)?

• Can DEA confirm these recordkeeping, prescription legend, and registration requirements only apply to those practitioners issuing a “telemedicine prescription” under 21 U.S.C. § 802(54)(G), and do not apply to other telemedicine prescribing of controlled substances? Do these proposed rules not apply if the practitioner meets a different Ryan Haight Act exception, or if the practitioner conducted a prior in-person exam and now is prescribing via telemedicine)?

• Should DEA use a different turn of phrase instead of “telemedicine prescription” to describe this new option and reduce industry confusion that it would more broadly apply to all prescriptions resulting from telemedicine?

• Is the proposed qualified telemedicine referral process fair and balanced? Should the referring practitioner be required to name a specific telemedicine doctor, or can the referring practitioner instead name a specialty group, hospital, or facility? If the referring practitioner names a specific practitioner, but he/she is unavailable, can a colleague in that same medical group take the referral?

• Are the proposed recordkeeping obligations feasible for practitioners, and will they result in benefits commensurate with the burdens?

• Why is there a 30-day limit on the initial prescription? Is that overly restrictive? Would an alternate maximum day supply be more appropriate than the one proposed in this rulemaking?

• How will DEA address multistate practice location registrations post-PHE?

• What additional flexibilities should be considered for this rule?

• Under the proposed rule, if a practitioner wishes to issue a “telemedicine prescription,” the practitioner must have a DEA registration in both the state where the patient is located and the state where the practitioner is located (i.e., even if the practitioner does not prescribe to patients located in that state, such as a vacation home).Does this proposed rule’s two-state registration requirement apply solely to those practitioners issuing “telemedicine prescriptions” under 21 C.F.R. § 1306.31 conducted pursuant to 21 U.S.C. § 802(54)(G)?Or does DEA this proposed rule’s two-state registration requirement apply to practitioners using other practice of telemedicine exceptions under the Ryan Haight Act?

• The proposed rule does not state what DEA will do with the current COVID-19 PHE waivers on DEA state-by-state practice location registrations, come May 11, 2023. Will the DEA will also apply a 180 day extension to its state-by-state registration requirements? If so, is that extension limited solely to prescriptions in connection with a telemedicine relationship established during the COVID-19 public health emergency?

• Does DEA have a proposal for practice location registration applications when the practitioner has a multistate telemedicine practice?

• In the proposed rule, it appears DEA wants a single location at which it can obtain records, and a way to conduct data monitoring and tracking of prescription patterns across multiple states. Is there a way to realize these goals in a much less complex rule structure?

Conclusion

The DEA proposed a complex rule with many technical features that will deeply affect a cohort of patients whose clinical care is dependent upon their medications.  The DEA gave the public only 30 days to comment on the proposals, after which DEA will prepare final regulations. Providers, facilities, technology companies, professional associations, and patients themselves must consider submitting comments to make your voices heard.