Good faith exam requirements in 2026 still depend heavily on the state, treatment, and provider involved. There is no single national rule that replaced every clinic’s existing process this year. The more important update is that clinics should not assume an exam workflow built in a previous year still satisfies current state requirements. Telemedicine clearance remains available in many states, but provider licensure, exam format, documentation, and treatment-specific requirements can differ.
Key Takeaways
- Good faith exam requirements remain state-specific and should be reviewed periodically as state rules and board guidance change. (Jump to Section)
- A virtual exam still needs to function as a real clinical evaluation, not simply a digital intake form. (Jump to Section)
- Short questionnaires and incomplete charting remain a major compliance weakness for med spas and wellness clinics. (Jump to Section)
- Existing templates should be reviewed to confirm they still capture the information needed to support the treatment decision. (Jump to Section)
- Multi-state clinics should review each state separately because provider and telehealth requirements can change by patient location. (Jump to Section)
What’s Changed in Good Faith Exam Rules for 2026?
The biggest 2026 takeaway is not a new national good faith exam standard. It is the continued importance of state-by-state review.
States use different terminology and rules for the evaluation that occurs before prescription-based aesthetic or wellness treatment. Requirements can differ in who may perform the exam, whether telemedicine is permitted, what technology is acceptable, and when another evaluation is required.
Medical Director Co.‘s current good faith exam guidance identifies these as the areas where states continue to differ most.
For clinics reviewing their process in 2026, check:
- Who performs the exam: Confirm that the clinician is authorized to evaluate the patient and make the treatment decision under the applicable state rules.
- Where the patient is located: Telehealth practice generally follows the patient’s physical location. The evaluating provider must be licensed or otherwise legally permitted to practice there.
- What type of remote encounter is permitted: Some states allow virtual evaluations under specified conditions, while others impose additional requirements.
- How the treatment is authorized: Confirm whether the state requires a patient-specific order, standing order, or another form of documented authorization for the service.
- When the exam must be repeated: Renewal requirements can depend on state law, treatment type, and changes in the patient’s condition.
The practical lesson for 2026 is simple: review the current rule instead of relying on the date your existing policy was written.
Is your good faith exam process still current?
Telemedicine Clearance: What Still Qualifies
Telemedicine can still be used for good faith exams in many states. The virtual format does not lower the clinical standard.
A compliant virtual encounter should allow the authorized provider to gather enough information to determine whether the patient is an appropriate candidate for treatment.
Medical Director Co.’s current virtual good faith exam guidance emphasizes live clinical evaluation rather than relying only on forms, texts, or automated questionnaires. State requirements can still differ, so clinics should confirm what their jurisdiction permits before making virtual clearance the default.
A virtual workflow should address:
- Provider authorization: The person performing the exam should have the license and authority required for the patient’s state.
- Patient location: Staff should document where the patient is physically located during the encounter.
- Clinical history: The provider should review relevant medical history, medications, allergies, contraindications, and current concerns.
- Actual clinical assessment: The encounter should give the provider enough information to make an individualized treatment decision.
- Treatment decision: The record should show whether the patient was approved, declined, or referred for further evaluation.
- Documentation: The virtual encounter should be documented as a clinical visit rather than reduced to a completed intake form.
Federal telehealth guidance also continues to treat licensure as state-based. HHS notes that providers generally must be licensed or legally permitted to practice in the state where the patient is located.
For a deeper breakdown, see Can a Good Faith Exam Be Done Virtually?.
Where Med Spas Get Good Faith Exams Wrong
A clinic can schedule the exam correctly and still create a compliance problem in the chart. One recurring issue is treating an intake questionnaire as if it were the medical evaluation itself.
A patient may complete questions about medications, allergies, previous procedures, and medical history before the visit. That information is useful, but it does not replace the provider’s clinical assessment and documented treatment decision.
Medical Director Co.’s documentation guidance recommends treating the good faith exam like another clinical encounter. The record should show the history reviewed, relevant findings, assessment, and plan rather than only a checked box that says the patient is “cleared.”
Other common gaps include:
- No clear treatment decision: The chart contains intake information but does not show why treatment was approved.
- Generic notes: Every patient’s record uses nearly identical language without documenting relevant individual findings.
- Missing provider information: It is unclear who actually performed the evaluation and made the clinical decision.
- No link between the exam and treatment: The record does not clearly identify the treatment the patient was evaluated to receive.
- Incomplete telehealth documentation: The clinic does not document that the encounter occurred remotely or where the patient was located.
- No renewal process: The clinic has no system for identifying when a new evaluation may be needed.
The goal is not more paperwork for its own sake. The chart should make the clinical decision understandable to someone reviewing it later.
Update Your Good Faith Exam Documentation for 2026
Clinics with an existing process do not necessarily need to rebuild it from the beginning. They should confirm that the current workflow still matches their services, providers, and states.
Start with the forms and templates your team actually uses.
Confirm the Patient Record Captures the Clinical Encounter
The record should contain enough information to show that a qualified provider evaluated the patient before treatment.
Review whether your template captures:
- Relevant medical history;
- Medications and allergies;
- Contraindications;
- Treatment being considered;
- Relevant clinical findings;
- Assessment of treatment suitability;
- Treatment approval or denial;
- Provider name and credentials; and
- The date of the evaluation.
Medical Director Co.’s current charting guidance recommends documenting the history, findings, assessment, and treatment plan that support the decision.
Review Telemedicine Fields
If exams are performed remotely, the documentation should reflect the remote encounter.
Check whether the record captures patient location, provider identity, the method of communication, and any other information required by the applicable state.
HHS telehealth guidance also recommends documenting telehealth encounters and maintaining appropriate clinical records.
Review the Workflow When Services Change
Adding a new service can change what needs to happen before treatment. A process designed around injectables may not automatically address IV hydration, prescription weight management, hormone therapy, or another treatment category.
Update your GFE process when the clinic adds:
- A new treatment;
- A new prescription medication;
- A new provider type;
- Another location; or
- Another state.
The exam process should follow the care being provided today, not the care the clinic offered when the template was first created.
Need to update your good faith exam process?
Multi-State Clinics Need More Than One GFE Workflow
A single corporate GFE policy can create problems when a clinic expands across state lines.
The patient may receive the same treatment at every location, but the rules governing the evaluation can still differ.
A multi-state clinic should confirm for each jurisdiction:
- Who can perform the exam;
- What license the provider needs;
- Whether telemedicine is permitted;
- What type of virtual encounter qualifies;
- How treatment authorization must be documented; and
- When another exam is required.
This becomes especially important when the same telehealth provider evaluates patients in several states.
HHS states that a telehealth appointment occurs in the state where the patient is located. Providers therefore need the appropriate authority to practice in each relevant jurisdiction.
Medical Director Co.‘s remote GFE guidance similarly recommends building multi-state workflows around the patient’s location rather than assuming one provider or one policy can be used nationwide.
When Should You Recheck Your Good Faith Exam Process?
A compliance review should not be limited to January simply because the calendar changed. Review the process when something changes that could affect who evaluates the patient or how treatment is authorized.
Useful review points include:
- Adding a new treatment category;
- Hiring an NP, PA, RN, or another clinical provider;
- Changing the clinician who performs remote exams;
- Expanding into another state;
- Changing telehealth platforms;
- Adding another clinic location;
- Revising standing orders; or
- Receiving new guidance from a medical or nursing board.
A periodic review is also useful even when the clinic has not changed. State board guidance and telehealth requirements can evolve while the clinic’s internal workflow stays the same.
How Medical Director Co. Keeps Good Faith Exams Current as Rules Change
Medical Director Co. helps clinics structure physician oversight around their services, providers, and states of operation.
Placed physicians can support good faith exam workflows, standing orders, clinical protocols, chart review, and other oversight responsibilities. Medical Director Co. also maintains state-specific compliance resources that clinics can use when their services or locations change.
Current plans start at $799 per month, with physician placement available within 24 hours.
For clinic owners, the advantage is ongoing support rather than treating good faith exam compliance as a one-time setup.
Keep your good faith exam process current.
FAQs
What changed in good faith exam requirements for 2026?
There is no single nationwide 2026 rule that changed good faith exams for every clinic. Requirements remain state-specific, so clinics should confirm current rules for provider authority, telemedicine, documentation, treatment authorization, and renewal.
Is a virtual good faith exam still valid in 2026?
Virtual good faith exams remain permitted in many states when the encounter meets applicable telehealth and clinical requirements. The provider must also be licensed or otherwise authorized to practice where the patient is located. State-specific restrictions should still be checked.
What’s the biggest good faith exam mistake med spas make?
One common problem is relying on an intake questionnaire or abbreviated checklist without documenting the provider’s actual clinical assessment and treatment decision. The medical record should show why the patient was approved or declined for treatment.
Does good faith exam documentation need to change in 2026?
Not every clinic needs a new form simply because the year changed. Review the existing documentation whenever state requirements, services, providers, locations, or telehealth workflows change.
Can the same good faith exam process be used in every state?
States differ in who can perform the evaluation, telehealth requirements, documentation expectations, and renewal rules. Multi-state clinics should review each jurisdiction individually.
Does a phone call count as a virtual good faith exam?
Do not assume that phone-only clearance satisfies the requirements in your state. Medical Director Co.’s current guidance recommends confirming whether the state requires synchronous video or another specific telehealth format before relying on remote clearance.
Who should review a clinic’s GFE documentation?
The medical director or another qualified clinician involved in the clinic’s oversight should understand how the exam is performed and documented. Legal or regulatory questions may also require review by appropriate healthcare counsel.
How does Medical Director Co. help clinics keep good faith exams compliant?
Medical Director Co. connects clinics with physicians who can support good faith exam processes and broader clinical oversight. The service can also support state-specific agreements, standing orders, clinical protocols, and ongoing compliance needs.
Keep Your Good Faith Exam Process Current
Good faith exam compliance should be reviewed as state requirements, providers, services, and telehealth workflows change. A process that worked previously should not be assumed to remain appropriate without periodic review.
Medical Director Co. can help clinics maintain physician oversight and update the clinical structure behind their good faith exam process.
Is your 2026 GFE process up to date?