Sarpatwari A, Brown BL, McGraw SA, Dejene SZ, Abdurrob A, Kesselheim AS - PLOS ONE
Interviewed physicians held mixed views on the impact of FDA risk evaluation and mitigation strategy (REMS) programs for drugs on their clinical practice, with many expressing concerns about the programs’ administrative burden and patient privacy. This suggests that while REMS programs may have positive features, they must be better integrated into clinical workflows.
VIEW SOURCE
Daval CJR, Kesselheim AS - STAT
Mulsant SS, Kesselheim AS, Naci H - Journal of Cancer Policy
Costa E, Kesselheim AS - Journal of Law, Medicine, & Ethics