Over the last decade, multiple initiatives have been undertaken to learn how to capture the carbon footprint of a supply chain at a product level. The purpose of this paper is to focus on the process of standardization to secure consistency of product carbon footprinting (PCF) and to outline how the current developments in PCF support the need for a standardized method to measure and report env…
The registration of medical devices is carried out by the Directorate General of Pharmaceutical Services and Medical Devices (Dirjen Binfar dan Alkes), within the MoH. The registration of medical devices is currently implemented through Regulation No. 1190/MENKES/PER/VIII/2010 Regarding Marketing Licence of Medical Devices and Household Products.