Pharmacy premises licensing policy formulation: experience from Ghana

Author:

Koduah AugustinaORCID,Sekyi-Brown Reginald,Nyoagbe Joseph Kodjo Nsiah,Danquah Daniel Amaning,Kretchy Irene

Abstract

Abstract Background Licences to operate pharmacy premises are issued by statutory regulatory bodies. The Health Institutions and Facilities Act (Act 829) and Health Professions Regulatory Bodies Act (Act 857) regulate pharmacy premises and the business of supplying restricted medicines by retail, respectively, and this could create a potential regulatory overlap for pharmacy practice in Ghana. We theorise that the potential overlap of regulation duties stems from how law-makers framed issues and narratives during the formulation of these Acts. Objective To describe the policy actors involved, framing of narratives and decision-making processes relating to pharmacy premises licensing policy formulation. Methods A qualitative study was conducted and data gathered through interviewing eight key informants and reviewing Hansards, reports, bills, memoranda and Acts 829 and 857. Data were analysed to map decision-making venues, processes, actors and narratives. Results The Ministry of Health drafted the bills in July 2010 with the consensus of internal stakeholders. These were interrogated by the Parliament Select Committee on Health (with legislative power) during separate periods, and decisions made in Parliament to alter propositions of pharmacy premises regulations. Parliamentarians framed pharmacies as health facilities and reassigned their regulation from the Pharmacy Council to a new agency. The Pharmacy Council and the Pharmaceutical Society of Ghana could not participate in the decision-making processes in Parliament to oppose these alterations. The laws’ contents rested with parliamentarians as they made decisions in venues restricted to others. Legislative procedure limited participation, although non-legislative actors had some level of influence on the initial content. Conclusion Implementation of these laws would have implications for policy and practice and therefore understanding how the laws were framed and formulated is important for further reforms. We recommend additional research to investigate the impact of the implementation of these Acts on pharmacy practice and business in Ghana and the findings can serve as bargaining information for reforms.

Publisher

Springer Science and Business Media LLC

Subject

Health Policy

Reference39 articles.

1. Government of Ghana. Health professions regulatory bodies act (Act 857). Accra: Ghana Publishing Company (Assembly Press); 2013a. p. 38–53.

2. World Health Organization. The legal and regulatory framework for community pharmacies in the WHO European Region. Copenhagen: World Health Organization; 2019.

3. Governor of the Gold Coast. The druggist ordinance. Accra: The State Publishing Corporation; 1892.

4. Koduah A, Sekyi-Brown R, Kretchy I. The evolution of pharmacy practice regulation in Ghana, 1892–2013. Pharm Hist. 2020;50(4):97–108.

5. Ministry of Health. The pharmacy and poisons ordinance. Accra: The State Publishing Corporation; 1946.

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