There is “more that can be done” by health technology assessment (HTA) bodies such as England’s NICE to ensure that real-world evidence (RWE) frameworks are consistent with those of other global agencies, Sarah Jenner, a principal at consulting firm IQVIA, said during a virtual Westminster Health Forum event.
In particular, greater standardization among HTA bodies on the acceptance of RWE could “help improve the speed and access to medicines through these quite lengthy HTA processes,” Jenner
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