On May 17, the U.S. Food & Drug Administration (“FDA”) issued two important draft guidance documents, which clarify the agency’s approach to requirements and incentives in the realm of.
FDA issued two new guidances on development and clinical trials of pediatric medications replacing 2005 rules. Pediatric drugs are developed slower difficulty clinical testing. Adult drugs can be used off label for children. New rules incentivize pediatric drug development.
/PRNewswire/ According to Prophecy Market Insights ""Gene Therapy for Rare Disease Market accounted for US$ 78.4 Million in 2022 and is estimated to be US$.