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Position Statements and Letters

Regarding the Practice of Homeopathic Medicine

About Licensed Homeopathic Physicians and Allied Healthcare Professionals

Licensed physicians have been prescribing homeopathic medicines in the course of their practice of medicine ever since 1810, when the homeopathic phenomenon was first elucidated, made public, and developed as a system of medicine by Dr. Samuel Hahnemann, a celebrated German physician.   His three major works are the Organon of Medicine (1810), the Materia Medica Pura (1821), and the Chronic Diseases (1828), all of which were written for physicians in their practice of medicine.   Homeopathic physicians are in practice throughout the world and homeopathy is officially recognized as a system of medicine by the national/government health services of the UK, France, Switzerland, and India, among others.

Since 1844, the American Institute of Homeopathy (AIH) has been the voice of the homeopathic medical profession in the United States.   Our membership comprises physicians (medical, osteopathic, naturopathic), dentists, veterinarians, nurse practitioners, physician assistants, pharmacologists and pharmacists all of whom have additional training in homeopathic medicine.  Licensure is a prerequisite to membership in the American Institute of Homeopathy.  

As licensed homeopathic physicians and allied healthcare professionals, we are bound by the law to adhere to the same standards of practice as corresponding mainstream licensed professional providers, though homeopathic therapeutic decisions are made in accordance with the principles of homeopathic medicine.   These standards of practice include the following:

  1. Taking a medical history and completing any necessary physical examination;  
  2. Obtaining appropriate laboratory and diagnostic studies;  
  3. Interpreting diagnostic studies and reviewing medical records;
  4. Assessing the urgency of the medical condition being treated and referring to appropriate specialists in a timely manner;
  5. Diagnosing and treating the patient in accordance with the licensure of the practitioner;  
  6. Monitoring the progress of the patient’s condition and modifying the treatment plan as needed;
  7. Maintaining appropriate medical records;
  8. Acquiring further training as required to maintain our respective licenses, in the form of continuing medical education courses and seminars;
  9. Practicing in accordance with a professional code of ethics and confidentiality.

Scope of Practice

We recognize that the Scope of Practice may differ for our different professions.   All of our members are committed to practice medicine/dentistry in accordance with the Scope of Practice specified by our respective licenses.

Legal Status of Homeopathic Medicines

Homeopathic medicines are included in the Food, Drug and Cosmetic Act of 1938 (see SEC. 201. (g)(1) of the Act 21 U.S.C. §321), and therefore fall within the regulatory authority of the FDA,  which recognizes the  Homeopathic Pharmacopoeia of the United States (HPUS) as their official compendium.    The  HPUS  is also recognized in the Controlled Substances Act (21 U.S.C. § 802).   Approximately 98% of homeopathic medicines are classified as non-prescription drugs.   See  www.hpus.com  for further information.  

Our members are duly licensed to prescribe medicines contained in the  USP  and  HPUS, in accordance with our respective DEA licenses.  

Safety of Homeopathic Medicines

While homeopathic medicines have an outstanding safety profile, absolute safety is not assured.   The homeopathic pharmaceutical industry adheres to rigorous standards and monitors the occurrence of adverse events.  Their data indicate that, while rates are extremely low, there are rare incidences of  Adverse  Events  and  Serious Adverse Events  associated with the use of homeopathic medicines.    

The Necessity of IRBs for Homeopathic Provings

A homeopathic proving refers to the experimental method by which the effects of homeopathic medicines on human subjects are discovered and documented.    As with all research that involves the administration of medicinal substances to human subjects, approval of the research by an Institutional Review Board (IRB) is mandated by federal legislation (see CFR, Title 45, Public Welfare, Department of    HHS, Part 46, Protection of Human Subjects, Subpart A, Section 46.101).    The AIH endorses only the HPCUS guidelines for Homeopathic Provingswhich include a requirement for IRB approval.  

Certification and Licensure

We encourage all our members to seek certification.  For licensed professionals, certification is a voluntary process that demonstrates to the public a specified level of expertise in one’s profession.   In contrast, licensure by the state is a requirement for the right to practice medicine, irrespective of whether or not the practitioner is certified.  

There are three certifying bodies for homeopathic practitioners in the United States:

1. Established in 1959, the American Board of Homeotherapeutics (ABHt) grants Board-certification in Classical Homeopathy as a Doctor of Homeotherapeutics (DHt) to licensed medical and osteopathic physicians who have graduated from an accredited medical or osteopathic school.

2. Established in 1988, the Homeopathic Academy of Naturopathic Physicians (HANP)   grants certification in Classical Homeopathy as a Diplomate of the HANP (DHANP) to naturopathic physicians who have graduated from an accredited naturopathic school.   See  www.hanp.net/membership/specialty for all requirements.

3. Established in 1991, the Council for Homeopathic Certification (CHC) grants certification as a Certified Classical Homeopath (CCH) to practitioners with no requirement for licensure and no requirement for graduation from an accredited health professions school.  Although some licensed practitioners choose to obtain certification through the CHC, the majority of CCHs are non-licensed homeopathic practitioners.   See www.homeopathicdirectory.com for all requirements.

Recent Position Statements and Letters

Access to Homeopathy Threatened by Latest FDA Action

The U.S. Food and Drug Administration (FDA) has recently proposed a new guidance regarding Homeopathic medicines that could have severe consequences on the survival of Homeopathy in the U.S.

The consequential action taken by the FDA involves the elimination of the administrative framework for homeopathy that the agency used for 30 years, one that allowed manufacturers of homeopathic remedies to thrive while ensuring the quality and purity of homeopathic medicines.

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Regarding the Practice of Homeopathic Medicine

Licensed physicians have been prescribing homeopathic medicines in the course of their practice of medicine ever since 1810, when the homeopathic phenomenon was first elucidated, made public, and developed as a system of medicine by Dr. Samuel Hahnemann, a celebrated German physician. His three major works are the Organon of Medicine (1810), the Materia Medica Pura (1821), and the Chronic Diseases (1828), all of which were written for physicians in their practice of medicine.

Read More »

Letter to FDA

On behalf of the American Institute of Homeopathy (AIH), we are respectfully submitting additional comments to the Food and Drug Administration (FDA) on the Draft guidance entitled “Drug Products Labeled as Homeopathic, Guidance for FDA Staff and Industry (Draft Guidance) issued December 20, 2017.    These comments incorporate and supplement the AIH comments submitted to the record on February 8, 2018.

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