In order to implement the implementation of integrated risk-based business licensing supervision as mandated in PP number 5 of 2021 concerning the implementation of risk-based business licensing, the Directorate General of Pharmaceuticals and Medical Devices, in this case represented by the Directorate of Medical Device Supervision, conducted a trial of risk-based business licensing supervision in the health sector together with the Coordinating Ministry for Economic Affairs and the Ministry of Investment / BKPM and involving the Department for Business, Energy & Industrial Strategy of the United Kingdom.
The activities held on February 22-24, 2023 in Bangka Belitung Province began with a visit to the Bangka Belitung Provincial Health Office and conducting coordination meetings related to the implementation of these activities. The trial activity was intended as a trial of incidental supervision of public complaints or findings from the government.
During the supervision visit, business actors provide data and information related to the development of their business and the obstacles encountered. The team then records information and conformity of business activities carried out with business licenses that have been submitted through the OSS system, the team also provides recommendations regarding problems that may be encountered, whether they have met the business requirements and standards for implementing business activities, whether guidance is needed, improvements or sanctions need to be applied. visit to the Bangka Belitung Provincial Health Office and conduct coordination meetings related to the implementation of these activities. The trial activity was intended as a trial of incidental supervision of public complaints or findings from the government.
In addition to conducting visits, the Directorate of Medical Device Supervision also conducted CDAKB socialization by involving the Bangka Belitung Provincial Office by inviting 12 Distributors of Medical Devices and PKRT both central and branch in the Bangka Islands region. It is hoped that through this meeting it can add insight, information and improve the quality of medical devices. awareness bagi para pelaku usaha terkait pengawasan perizinan.