Bailiwick News • 1783 implied HN points • 09 Oct 24
- From 1911 to 1943, U.S. Congress didn't create laws to establish clear definitions or standards for biological products, like vaccines and toxins. This meant there were no guidelines for safety or labeling requirements.
- The 1902 Virus-Toxin Act only focused on the licensing of manufacturers, not the products themselves. This led to a lack of oversight on what was in those products and whether they were safe to use.
- Even with new regulations in later years, there was still confusion and gaps in laws about the safety and efficacy of biological products, allowing manufacturers to operate without strict requirements.