The FDA's initiative can provide faster market access for SpectraCure
During SpectraCure's ongoing clinical trial, the American FDA (Food and Drug Administration) has created an opening for faster product launch by changing the requirements for endpoints in clinical trials in cancer treatment. The changed requirements provide new opportunities that in the long term may entail faster market access. The FDA's initiative to admit shorter follow-up times and accelerated approval, is supplemented with requirements for reporting follow-up studies after approval. SpectraCure may launch its treatment system as early as 2020/2021 after approval by the FDA, with the