In accordance with the mandate of Minister of Health Regulation No. 28 of 2023 concerning the Organization and Work Procedures of the Technical Implementation Unit (UPT) for the Safety of Devices and Health Facilities, the Directorate General of Pharmaceuticals and Medical Devices fully fosters and coordinates the UPT for Safety of Devices and Health Facilities (PAFK).
The Minister of Health Regulation stipulates that administrative guidance is under the coordination of the Secretary of the Directorate General and functional technical guidance is under the coordination of the Technical Director in this case the Director of Medical Device Supervision as stated in the directive indicators in the performance agreement.
Therefore, in carrying out these duties and functions, at BPAFK Surakarta on February 7, 2024, the Secretary of the Directorate General of Pharmacy and Health along with the Directors within the Directorate General of Pharmaceuticals and Health Equipment held guidance and coordination with BPAFK / LPAFK.
On the same occasion, Director General of Pharmaceuticals L.Rizka Andalucia submitted the Performance Agreement that had been determined to Echelon II of the Central Satker and the Head of BPAFK / LPAFK within the Directorate General of Pharmaceuticals and Medical Devices.
The performance agreement was prepared based on the Regulation of the Minister of Administrative Reform and Bureaucratic Reform Number 53 of 2014 concerning Technical Guidelines for Performance Agreements, Performance Reporting and Procedures for Reviewing Government Agency Performance Reports.
Rizka in her speech said that in preparing the program, it is expected not only to carry out tasks and functions, but there is a need for innovation, especially for work units and UPTs that carry out public services. "The head office and UPT within the Directorate General of Pharmaceuticals and Medical Devices have their own important roles in achieving health development goals in the pharmaceutical and medical device sectors," said Rizka.