The United States Agency for International Development (USAID), the National Planning Department (DNP), the Ministry of Health and Social Protection (MinSalud), the Ministry of Commerce, Industry and Tourism (MinCIT), the National Institute of Vigilance od Medicines and Food (INVIMA) through the Directorate of Medical Devices and Other Technologies, the Medical Devices and Health Supplies Chamber at ANDI and the Inter-American Coalition for Regulatory Convergence, Medical Technology Sector (IACRC), organized a Workshop on the “Experience on the Regulatory Impact Analysis -Problem Tree- for Good Manufacturing Practices of Medical Devices” where the MoH shared their expierience while building it and its evolution throughout the process, as part of the activities organized under the MDRC Project.
You can find the session´s materials in the following links:
