Manufacturing and Industry
Ministry of Health Regulation No. 62 of 2017 on Distribution Licenses for Medical Devices, In-Vitro Diagnostic Medical Devices and Household Medical Supplies
Enforcement Date: 12 January 2018
Any medical devices, in-vitro diagnostic medical devices and household medical supplies which are manufactured, imported, assembled and/or repackaged for distribution in Indonesia are first required to secure distribution licenses (“Distribution License”) from the Directorate-General of Pharmaceuticals and Medical Devices (“Directorate-General”).
Sets out detailed provisions regarding procedures for the securing of Distribution Licenses, comprising: 1) Application processing (i....
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