Ref. Gnegel, G., Häfele-Abah, C., Neci, R. et al. Surveillance for substandard and falsified medicines by local faith-based organizations in 13 low- and middle-income countries using the GPHF Minilab. Sci Rep 12, 13095 (2022). https://doi.org/10.1038/s41598-022-17123-0 Dear Colleagues, This interesting manuscript from our friends of EPN and University of Tubingen, evaluates the use of the Global Pharma Health Fund (GPHF) Minilab ...
On 28 September, the SPF Public Health, in collaboration with the SPF Foreign Affairs, ITM, the Be-Cause Health platform and the NGO IYAD, is organising a conference entitled:“Pain therapy in D.R. Congo. A neglected element in the process of UHC of a weakened health system”. Please find the programme below. The purpose of this meeting ...
QUAMED’s board of directors is happy to announce that it has appointed Mr Tahina Andrianjafy as the chair of its internal audit committee. It is expected that he will continue in that capacity for a period of 3 years. Mr Andrianjafy brings 25 years of experience in the management and implementation of pharmaceutical supply chains programs. He ...
In 2021, we were fortunate to welcome new members, with 29 organisations and 23 individual members. Our activities have also increased significantly from just 1 single audit in 2020 to 8 MQAS audits, 10 GSDP audits and 76 GSDP technical visits in 2021. We are pleased to share our QUAMED Annual Report of 2021. Both ...
Over the past 2 years, QUAMED has invested in developing its quality management system (QMS). Our QMS manual, procedures, and policies that are part of the QMS are all based on the QUAMED quality policy. This policy includes our commitment to continually improving our QMS. It also provides a framework to set quality objectives and ...
Our pilot virtual course “Inspection of medical products distributors against WHO GSDP”, is well underway and will continue until the end of August 2022. We developed this course for PAHO. The target group for the course are the NRA staff in the Latin American and the Caribbean (LAC) region. The English group includes 18 participants ...
QUAMED as a member of Team Belgium is continuing to prepare technical support for the Rwanda FDA (www.rwandafda.gov.rw). For that purpose, we are looking for a regulatory expert who has strong experience and expertise, specifically in dossier assessments and registration, Market Surveillance, GMP Inspections and Pharmacovigilance. The expert has to have at least 10 years ...
On Monday, the 28th of February, our auditor Jean-Christophe Pelissier has worked with the Agence Congolaise de Réglémentation Pharmaceutique (ACOREP) in DRC. He facilitated training on Good Storage and Distribution Practices and how to conduct a Pharmaceutical Inspection and Audit. There were 33 participants in the training. As a follow-up to the training, Mr Pelissier ...
Last week we held our first two QUAMED webinars of the year, in both English and French, with 36 people attending. The webinar topics were the #EudraGMDP database, presented by Valérie Solbes of MdM France and Didier Morellet of Première Urgence Internationale, and the USFDA medical devices databases, presented by Aida Cancel and Alexandra Guta from #FHI360 – thank you to the excellent presenters! Our #WebinarSeries will continue ...
Our GSDP auditor, Mr Alex Kosyak (4th from left), has successfully finalised 3 #GSDP #audits in Zambia. He is shown here with the staff of Sterelin Medical & Diagnostics, one of the three suppliers that were audited.
Would you like more information about audits or get a quote? Do not hesitate to contact us via the contact form.
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