The Utility of a Rapid Review Evaluation Process to a National HTA Agency

Author:

Varley ÁineORCID,Tilson Lesley,Fogarty Emer,McCullagh Laura,Barry Michael

Funder

University of Dublin, Trinity College

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health,Health Policy,Pharmacology

Reference19 articles.

1. Government of Ireland (Oireachtas). Health (Pricing and Supply of Medical Goods) Act 2013, Number 14. Irish Statute Book. Dublin: Office of the Attorney General; 2013. http://www.irishstatutebook.ie/eli/2013/act/14/schedule/3/enacted/en/html#sched3. Accessed 4 Oct 2021.

2. Barry M, Heerey A, Hughes C, McCulloch D, Merry C, Ryan M, et al. The Irish National Centre of pharmacoeconomics: its rationale and role. IMJ. 1999;92(4):337–9.

3. Directive 2013/50/EU of the European Parliament and of the Council of 22 October 2013 amending Directive 2004/109/EC of the European Parliament and of the Council on the harmonisation of transparency requirements in relation to information about issuers whose securities are admitted to trading on a regulated market, Directive 2003/71/EC of the European Parliament and of the Council on the prospectus to be published when securities are offered to the public or admitted to trading and Commission Directive 2007/14/EC laying down detailed rules for the implementation of certain provisions of Directive 2004/109/EC. OJ L 294, 6.11.2013, p. 13–27. https://eurlex.europa.eu/legal-content/EN/TXT/?uri=uriserv%3AOJ.L_.2013.294.01.0013.01.ENG&toc=OJ%3AL%3A2013%3A294%3ATOC. Accessed 4 Oct 2021.

4. Irish Pharmaceutical Healthcare Association, Health Services Executive. Framework agreement on the supply and pricing of medicines 2016. 2016. https://www.hse.ie/eng/about/who/cpu/iphaagreement2016.pdf. Accessed 23 Sep 2021.

5. McCullagh L, Barry M. The pharmacoeconomic evaluation process in Ireland. Pharmacoeconomics. 2016;34(12):1267–76.

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