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Category: Healthcare Regulatory Compliance

Articles on building and maintaining a compliant healthcare practice. Topics cover HIPAA compliance, fraud, waste, and abuse programs, good faith estimates, informed consent, controlled-substance and procedure SOPs, and patient intake policies and procedures, written for owners putting policies and procedures in place.

Physician at his desk reviews a bound study protocol, considering whether his small practice can run a clinical trial.

Can a Small Practice Run a Clinical Trial?

Clinical research is no longer limited to large hospitals and academic medical centers. Small medical practices can participate in clinical trials. Doing so requires careful attention to FDA regulations, IRB oversight, informed consent, HIPAA compliance, and liability management.

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Physician wearing a Medical Doctor name badge, illustrating disclosure rules for non-physicians using the Dr. title.

Misusing the “Dr.” Title: What Are the Risks, and How Can Supervising Physicians Avoid Them?

When non-physicians with doctoral degrees use the title “Dr.” in clinical settings, both the practitioner and the supervising physician can face regulatory scrutiny, fines, and disciplinary action. This post outlines how state title-use laws apply, what supervisory liability looks like in practice, and how reviewing collaborative agreements, supervision policies, and marketing materials can protect your practice.

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