Homeopathic Drugs Manufacturing
GMP Labs has been making homeopathic drug products since our inception in 1994, specializing in dry product forms such as tablets and two-piece capsules.
We strictly adhere to OTC drug manufacturing requirements of the FDA (CFR Part 211) as well as the traditional practices and guidelines set forth in the Homeopathic Pharmacopoeia of the United States (HPUS). As part of our compliance with CFR Part 211, GMP Labs has been granted an OTC drug license. Learn more about our certifications.