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. 2022 Jun 13;6(3):1726.
doi: 10.23889/ijpds.v6i1.1726. eCollection 2021.

The Medicines Intelligence Centre of Research Excellence: Co-creating real-world evidence to support the evidentiary needs of Australian medicines regulators and payers

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The Medicines Intelligence Centre of Research Excellence: Co-creating real-world evidence to support the evidentiary needs of Australian medicines regulators and payers

Nicole Pratt et al. Int J Popul Data Sci. .

Abstract

Regulators and payers play a pivotal role in facilitating timely and affordable access to safe and efficacious medicines. They use evidence generated from randomised clinical trials (RCTs) to support decisions to register and subsidise medicines. However, at the time of registration and subsidy approval, regulators and payers face uncertainty about how RCT outcomes will translate to real-world clinical practice. In response to this situation, medicines policy agencies worldwide have endorsed the use of real-world data (RWD) to derive novel insights on the use and outcomes of prescribed medicines. Recent reforms around data availability and use in Australia are creating unparalleled data access and opportunities for Australian researchers to undertake large-scale research to generate evidence on the safety and effectiveness of medicines in the real world. Highlighting the critical importance of research in this area, Quality Use of Medicines and Medicine Safety was announced as Australia's 10th National Health Priority in 2019. The National Health and Medical Research Council, Medicines Intelligence Centre of Research Excellence (MI-CRE) has been formed to take advantage of the renewed focus on quality use of medicines and the changing data landscape in Australia. It will generate timely research supporting the evidentiary needs of Australian medicines regulators and payers by accelerating the development and translation of real-world evidence on medicines use and outcomes. MI-CRE is developing a coordinated approach to identify, triage and respond to priority questions where there are significant uncertainties about medicines use, (cost)-effectiveness, and/or safety and creating a data ecosystem that will streamline access to Australian data to enable researchers to generate robust evidence in a timely manner. This paper outlines how MI-CRE will partner with policy makers, clinicians, and consumer advocates to leverage real-world data to co-create real-world evidence, to improve quality use of medicines and reduce medicine-related harm.

Keywords: MI-CRE; health policy; knowledge translation; partnership; pharmacovigilance; quality use of medicines; real world evidence; safety.

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Conflict of interest statement

Conflicts of Interest: CEB is a member of the Pharmaceutical Benefits Advisory Committee (PBAC); SP, NP, TL and CEB are members of the Drug-Utilization Sub-Committee of the PBAC; TL is a member of the Economics Sub-Committee of the PBAC; SP is a member of the National Data Advisory Council; CMV is Deputy Chair of the NSW Population Health Service Research Ethics Committee; DP is a member of the Sax Institute Board. The views of authors expressed in this review article are their own and do not represent those of the aforementioned bodies. In 2020, the Centre for Big Data Research in Health received funding from AbbVie Australia to conduct post-market surveillance research. AbbVie did not have any knowledge of, or involvement in, this manuscript.

Figures

Figure 1: MI-CRE Governance Structure
Figure 1: MI-CRE Governance Structure
Figure 2: MI-CRE research – policy pipeline and enablers for accelerating RWE development in Australia
Figure 2: MI-CRE research – policy pipeline and enablers for accelerating RWE development in Australia

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