Welcome to OHM

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QUALITY

"Quality is not an accident; it is always the result of high intention, sincere effort, intelligent direction and skillful execution; it represents the wise choice of many alternatives."

Quality for manufacturing homeopathic medicines starts at the site location. Our shielded facility has 18 inches steel reinforced concrete walls, protecting it from the elements and insulating it from electromagnetic disturbances. We also have an underground level making it the ideal manufacturing site for the purest homeopathic remedies. We are one hour and fifteen minutes from Dallas/Fort Worth airport, in the countryside, in a pollution-free environment.
OHM provides homeopathic medicines made with individual care, using traditional methods complying with current Good Manufacturing Practices (cGMP). We implement high-quality standards for manufacturing medicines in strict accordance with the Food and Drug Administration (FDA) and the Homeopathic Pharmacopoeia of the United States (HPUS).
OHM is a registered FDA establishment and Health Canada registered. Standardizing the manufacturing processes guarantees optimal reliability and reproducibility of the dilutions.

  • Our major laboratory equipment includes:
    TOC (Total Organic Compound) analyzer for purified water testing.
  • FT-IR spectrometer (identification testing).
  • IR-UV spectrometer (identification testing).
  • TLC chromatography (identification testing).
  • HPLC chromatography (identification and assay testing).
  • ICP-OES Inductively coupled plasma with optical emission spectrometry (heavy metal testing).
  • GC-FID Chromatography (identification and quantification of ethanol).
  • GC-ECD Chromatography (identification and quantification of pesticides).
  • Microbial Limit Tests applicable for each dosage form (Total Anaerobic Plate Count, Total Yeast and Mold Count, E. Coli, Salmonella, Staphylococcus, Pseudomonas). Suitability testing.
  • Physical testing (organoleptic tests, pH, specific gravity, alcohol content, viscosity, disintegration, breaking force, weight, size and thickness, rotation index, friability).
  • Stability testing in environmental chambers (accelerated and long-term storage conditions).
  • Other testing is performed as needed.

All validated and approved methods used for testing are based on the HPUS, USP/NF, or other pharmacopeias monographs.

Remedies are manufactured in strict accordance with cGMP, FDA and HPUS.