Good Faith Exam
for TRT

$26.99 Per Exam

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Testosterone replacement therapy is a controlled substance prescription. Every TRT prescription requires a documented clinical evaluation from a licensed provider before it is issued. A good faith exam for TRT is that evaluation. It is the step that creates the clinical foundation for the prescription, establishes the patient-provider relationship, and protects the practice from the regulatory exposure that comes with prescribing controlled substances without proper documentation.
GoodFaithExams.com makes that step available online through a licensed physician so practices prescribe with confidence and every patient starts treatment on a defensible clinical record.

What Is a Good Faith Exam for TRT

Testosterone is a Schedule III controlled substance. That classification carries the strictest prescribing documentation requirements of any category covered in this platform. A licensed provider must evaluate the patient, document the clinical basis for the prescription, and establish a valid patient-provider relationship before testosterone is prescribed in any form.

A good faith exam for TRT is a medical evaluation conducted by a licensed physician before a testosterone prescription is issued. The physician reviews the patient’s health history, current medications, relevant labs where available, prior testosterone therapy history, prostate health indicators, cardiovascular risk factors, and any conditions that affect how testosterone is metabolized or how the patient will respond to exogenous hormone supplementation.


Contraindications for TRT are specific and clinically significant. Prostate cancer or elevated PSA, polycythemia, untreated sleep apnea, and certain cardiovascular conditions are among the factors that require careful review before testosterone is prescribed. TRT good faith exam documentation creates the record that demonstrates a licensed provider reviewed this patient, for this controlled substance, and made an independent clinical decision.


GoodFaithExams.com delivers that documentation online. Patients complete intake on their own time. Practices receive documented clinical findings without adding overhead to a controlled substance prescribing workflow.

Why TRT GFE
Requirements Exist

Testosterone is a Schedule III controlled substance under the DEA. The prescribing standard for controlled substances requires a licensed provider to establish a valid patient-provider relationship and conduct a documented clinical evaluation before a prescription is issued. This requirement is federal, not just state-level.
TRT GFE requirements exist because testosterone prescribing has expanded significantly in men’s health and telehealth settings where same-day prescribing through intake forms has drawn DEA and state medical board attention. Practices issuing testosterone without documented clinical evaluation carry real federal and state regulatory exposure.
A documented good faith exam creates the defensible clinical record that separates a compliant TRT prescription from one that carries exposure.

Who Can Perform It

The provider conducting the exam must hold DEA registration and prescribing authority for controlled substances within their scope of practice. In most states, qualified providers include physicians, nurse practitioners with prescribing authority for controlled substances and appropriate supervision agreements, and physician assistants with controlled substance prescribing authority and appropriate supervision agreements.
GoodFaithExams.com connects patients with licensed physicians who meet state-specific controlled substance prescribing requirements. Every exam reflects independent clinical judgment.

What to Expect

Patient Intake

Patients submit health history, prior testosterone therapy history, relevant labs where available, prostate health indicators, cardiovascular history, and current medications.

Provider Evaluation

A licensed physician reviews the case through the platform.

Clinical Decision

The provider approves, modifies, or declines the prescription based on independent clinical judgment and contraindication review.

Documented Outcome

Each evaluation is recorded and delivered to the practice as a completed compliance record.

How GoodFaithExams.com Makes It Simple

An online GFE for TRT through GoodFaithExams.com is built for men’s health and hormone practices managing active testosterone prescribing volume under controlled substance regulations.
Available Monday Through Sunday. No DEA registration required on the practice side for evaluation purposes.
A good faith evaluation for TRT on GoodFaithExams.com reviews prostate health indicators, cardiovascular risk, hematocrit and polycythemia risk, sleep apnea history, prior testosterone response, and the full medication interaction profile relevant to exogenous testosterone supplementation. Calibrated for controlled substance prescribing standards.
A telehealth good faith exam for TRT is conducted by a licensed physician with controlled substance prescribing authority reviewing each patient individually. No automated clearances. Every finding is documented before the prescription is supported.

Pricing

$26.99 per exam.

No hidden fees. No monthly minimums. No contracts.

Who This Is and Is Not For

Good fit:

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Ready to Get Started

TRT patients are making a long-term commitment to their health. A good faith exam for TRT through GoodFaithExams.com makes sure that commitment starts with a proper clinical evaluation and a compliance record that holds up under the scrutiny that controlled substance prescribing attracts.
Start today at GoodFaithExams.com.

Frequently Asked Questions

What is a good faith exam for TRT?

A good faith exam for TRT is a required medical evaluation conducted by a licensed physician before a testosterone prescription is issued. It reviews health history, prior TRT experience, relevant labs, prostate and cardiovascular status, and contraindications specific to exogenous testosterone supplementation, and establishes the patient-provider relationship required before a controlled substance prescription can be defensibly written.
Testosterone is a Schedule III controlled substance under the DEA. That classification places TRT prescribing under federal controlled substance regulations in addition to state medical board requirements. The documentation standard for controlled substances is stricter than for non-controlled hormones, and non-compliance carries federal enforcement consequences, not just state board review.
TRT GFE requirements at the federal level require a licensed provider with DEA registration to establish a valid patient-provider relationship and conduct a documented clinical evaluation before testosterone is prescribed. State-level requirements add supervision, scope of practice, and documentation standards depending on the provider type and delivery model.
The reviewing physician looks at prostate cancer history or elevated PSA, polycythemia or elevated hematocrit, untreated obstructive sleep apnea, uncontrolled cardiovascular disease, infertility concerns, concurrent anticoagulant use, and prior adverse reactions to testosterone. Each factor affects whether TRT is appropriate at all, and at what dose and delivery format.
Lab results are clinically relevant and should be submitted when available. The reviewing physician will note the presence or absence of baseline labs as part of the clinical record. Practices should confirm their workflow for managing lab requirements under the applicable state and federal prescribing standards for controlled substances.
It creates a documented clinical record showing a licensed physician with DEA registration evaluated the patient, reviewed TRT-specific contraindications, and made an independent prescribing decision before testosterone was issued. That record is what DEA investigators and state medical boards ask for when reviewing controlled substance prescribing at men’s health and hormone clinics. decision before testosterone was issued. That record is what DEA investigators and state medical boards ask for when reviewing controlled substance prescribing at men’s health and hormone clinics.
A good faith evaluation for TRT is the clinical process through which a licensed physician with controlled substance prescribing authority assesses whether a patient is an appropriate candidate for testosterone replacement therapy, reviews contraindications and interaction potential, and documents an independent decision before the prescription is written. decision before testosterone was issued. That record is what DEA investigators and state medical boards ask for when reviewing controlled substance prescribing at men’s health and hormone clinics.
The evaluation reviews the patient’s suitability for testosterone replacement therapy and the clinical appropriateness of the specific delivery format being considered. Injectable, topical, and pellet formulations carry different considerations around absorption, frequency, and patient-specific factors. The reviewing physician accounts for delivery format as part of the clinical assessment.
Good faith exam telemedicine for TRT is the completion of a required pre-prescribing controlled substance evaluation through a remote digital platform. GoodFaithExams.com provides this through licensed physicians with DEA registration who review every patient individually and document independent clinical findings before TRT is prescribed.
A telehealth good faith exam for TRT conducted through GoodFaithExams.com is performed by a licensed physician with DEA registration. The evaluation documents the patient-provider relationship, clinical findings, and the prescribing decision. This aligns with the DEA’s extended telehealth prescribing flexibilities currently in effect through 2026 and supports compliance with state-level controlled substance prescribing requirements.

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