On Tuesday, April 21st, I was at FDA headquarters in Maryland to testify at a two day hearing the FDA was holding titled: “Homeopathic Product Regulation: Evaluating the FDA’s Regulatory Framework after a Quarter-Century“. The public, medical professionals and industry-related personnel were invited to apply to testify at the hearing. The hearing was open to all, and the majority of the people who spoke at the hearing had positive statements about homeopathy, its’ safety and its use as an over-the-counter medicine.
What I found fascinating was the reports in the mainstream media during the first day of testimony focused on the dangers of homeopathy, and the FDA’s issues with homeopathy being available to the public. A common theme in these news stories was that only advocates of homeopathy were testifying. This theme was not what was presented at the hearing and anyone was allowed to apply to testify. This was not why FDA had the hearing. This goes to show that you cannot always rely on the mainstream news outlets to present a fair, unbiased view.
Here is a link to the FDA website where you can watch the two days of testimony, hear questions the FDA asked the speakers, and also see who was asked by the FDA to testify. During the hearing, there was mention about a few products that were cited by the FDA for possible side effects or interactions. The FDA explained that when the investigated these products, they found that they were labeled as homeopathic products, but were NOT homeopathic products.
Media reports have neglected to mention that they were mislabeled and were not homeopathic products after all. Isn’t it strange that the story in the news and what actually went on at the hearing were so different? You now can see for yourself what really went on at the hearing. By reviewing the testimony, you will understand that the homeopathic community and the FDA are working together to ensure that the public has adequate information available to make educated decisions. Also addressed was a concern that the consumer may benefit from more information being on the OTC packages.
It was an honor to be asked to represent Johnson Compounding and Wellness and our customers at this hearing. This experience renewed my faith that everyone can work together to make sure the public has available quality products to choose, and quality information to educate themselves.
What is transfer factor? First discovered by immunologist H. Sherwood Lawrence in 1949, transfer factors are immune messenger molecules comprised of amino acids. In mammals