The MDRC is working through a multi-stakeholder approach and via an inter-agency collaboration with the Kenyan Pharmacy and Poisons Board (PPB), the Kenya Bureau of Standards KEBS), Customs and Border Control (KRA), MECOMED and the Medical Technology Industry Association (MEDAK) and other stakeholders and has identified the following MDRC priority areas of work in Kenya:

Good Regulatory Practices – Implementation and Operationalization
Use of international standards and conformity assessment as essential GRP
Medical Device Regulatory Convergence, Reliance and Recognition