Homeopathy is based on the system that ‘Like cures Like,’ and that the more dilute a drug is, the more potent it becomes, i.e. ‘The Law of Infinitesimals.’ Homeopathic Drugs have a long and storied tradition in the United States and include a myriad of products, dilutions, and potencies. The Homeopathic Pharmacopoeia of the United States (HPUS) is the official compendium for Homeopathic Drugs in the United States recognized in the Federal Food, Drug and Cosmetic Act (FDCA). Homeopathic drugs have a unique regulatory history that poses important challenges in manufacturing and marketing, distinct from Allopathic Drugs, Dietary Supplements, and Medical Foods. In fact, Homeopathic Drugs include a number of critical requirements separate from other products that demand specialized counsel.
Fuerst Ittleman is a leading law firm advising clients on issues concerning Homeopathic Drugs, FDA compliance, and product safety. We can assist with matters involving the need for premarket approval and postmarketing regulation (current Good Manufacturing Practices (cGMPS), marketing, and sales). Attorneys at Fuerst Ittleman have experience and skill directing product labels, advertising, reimbursement, prescribing, extemporaneous compounding, importation, state regulation of Homeopathic Drugs and response to FDA Warning Letters.
For more information on how we can assist with homeopathic drugs, please contact us at contact@fuerstlaw.com.
