SIAPS has been providing technical assistance to DGDA to improve its regulatory function by helping them adopt international standards for medicine registration based on a common format proposed by the International Council for Harmonization for Technical Requirements for Pharmaceuticals for Human Use (ICH), known as the Common Technical Document (CTD). The use of the format … Read more
As a part of its ongoing support to build the capacity of the DGDA, the Systems for Improved Access to Pharmaceuticals and Services (SIAPS) team conducted a rapid assessment of the capacity of the Good Manufacturing Practices (GMP) inspection program at the Directorate General of Drug Administration (DGDA). GMP is part of the quality assurance … Read more
Assessment, Bangladesh, Directorate General of Drug Administration, E Kim, Good Manufacturing Practices (GMP), governance, Inspection, J Aimiuwu, M Thumm, MH Anisfeld, Quality Assurance, regulations, SOPs
