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The effect of the Covid-19 pandemic has worsened inequitable access to health care systems in Africa and the world, Health Minister, Kwaku Agyeman-Manu, has said.<\/p>\n
He said the vulnerable populations continued to face higher burden of morbidity and mortality.<\/p>\n
The Minister was speaking at the opening of the 3rd African Medicine Regulatory Harmonization (AMRH) Week in Accra, on the theme: \u201cThe African Medicine Regulatory Harmonization \u2013 A foundation for the African Medicines Agency\u201d.<\/p>\n
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According to him, this situation was due to limited access to affordable,\u00a0effective\u00a0and\u00a0good quality\u00a0essential health care products and services in the African continent.<\/p>\n This he said could only be addressed through efficient and well coordinated efforts to harmonize regulatory processes and initiatives that would enhance collaboration among regional communities.<\/p>\n He said: \u201cMany African governments have realised and agree that there is an urgent need to strengthen manufacturing capacities on the continent for vaccines and other medical products as part of building strengthened health systems after the Covid-19 pandemic and in preparation for future pandemics should they occur\u201d.<\/p>\n Dr. David Mukanga, Deputy Director, Africa Regulatory Systems, expressed commitment to support the vision of the AMRH in addressing the challenges to achieve its objectives, adding that there was the need to move quickly due to Africa\u2019s many challenges.<\/p>\n \u201cWe need to move beyond plans and ideas to executing, and we are here to work with the African continent to make sure that people of the continent, mothers, children and the men on the street have access to quality medicines,\u201d\u00a0he said.<\/p>\n Mrs Delese Mimi Darko, Chief Executive Officer, Food and Drugs Authority (FDA), said Ghana, Egypt, Tanzania, South\u00a0Africa\u00a0and Nigeria were the African countries with strong regulatory systems.<\/p>\n She disclosed that the Authority had trained more than 52 African regulators in clinical trial oversight, pharmacovigilance, and marketing authorisation.<\/p>\n \u00a0She said: \u201cSince 2020, we have been designated as a Maturity Level 3 agency based on the World Health Organization\u2019s Global Benchmarking Tool and we are working assiduously to achieve ML4\u201d.<\/p>\n Mrs Darko noted that the momentum for joint learning and mentorship was rife and keen to grow along with many National Regulatory Authorities ( NRAs) to achieve the vision of a robust medicine regulatory regime in Africa.<\/p>\n The AMRH week is an event convened every two years by the AMRH joint secretariat which comprises the African Union Development Agency-NEPAD (AUDA-NEPAD) and the World Health Organisation (WHO) with support from the African Union Commission (AUC).<\/p>\n The \u2018week\u2019 brings together high-level African leaders and policy makers , members of the AMRH steering committee, Regional Economic Communities (REC) and other partners and stakeholders to\u00a0showcase\u00a0and celebrate the successes of AMRH as well as to reflect on progress, challenges and identify opportunities for continued improvement.<\/p>\n The NRAs across the globe, especially in Africa and other low and middle-income countries faced many challenges in ensuring access to quality medical devices , in-vitro diagnosis, personal protective equipment\u00a0 and other health products to control\u00a0 the COVID-19 pandemic.<\/p>\n In response to these challenges, AMRH steering committee is expected to provide accelerated technical support and assistance to address some of the challenges highlighted.<\/p>\n The 3rd AMRH week celebration which was hosted for the first time in Ghana would present an opportunity to share experiences, good\u00a0practices\u00a0and innovative responses to the pandemic by the NRAs.<\/p>\n The vision of the AMRH would ensure that countries work together under the AMRH, pull talents from across the continent, ensure best practices in regulatory processes while ensuring that medical products that are either produced locally or imported would be safe and of\u00a0good quality\u00a0for the citizenry.<\/p>\n <\/p>\n