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- W2953205965 abstract "Background: Improving access to new and established medicines for rheumatological disease is of public health importance. However, drug development processes, medicines regulation and health technology requirements may significantly impact on when a new medicine become available to be used by health care professionals. Objectives: The objectives of this session are to present some of the challenges and opportunities for accessing new and established medicines for rheumatological disease. Methods: Drug development processes, medicines regulation and health technology requirements may significantly impact on when a new medicine become available to be used by health care professionals. Although these requirements may be perceived as barriers, many of these requirements are in place to ensure a medicines benefit risk profile is favorable and is cost effective in terms of quality of life. This session will briefly discuss issues around the process of making medicines newly available from drug development to gaining new market approvals with an emphasis on rheumatological disease, including the post-authorization safety requirements that are in place to safe guard public health. Disclosure of Interests: None declared" @default.
- W2953205965 created "2019-06-27" @default.
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- W2953205965 date "2019-06-01" @default.
- W2953205965 modified "2023-09-27" @default.
- W2953205965 title "SP0123 NEW TREATMENTS: WHY SHOULD WE WAIT?" @default.
- W2953205965 doi "https://doi.org/10.1136/annrheumdis-2019-eular.8542" @default.
- W2953205965 hasPublicationYear "2019" @default.
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