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The Indonesian Food and Drug Authority (Indonesian: Badan Pengawas Obat dan Makanan, lit. 'Food and Drug Supervisory Agency'), Badan POM/BPOM, or Indonesian FDA is a government agency of Indonesia responsible for protecting public health through the control and supervision of prescription and over-the-counter pharmaceutical drugs (medication), vaccines, biopharmaceuticals, dietary supplements ...
Commonly, the minister usually came from medical doctor, however some of them were military doctor. Since 2009, the government has been required to allocate 5% of state budget for health sector. However, the mandatory 5% state budget for health sector was achieved in 2019. [1]
The NMPA is responsible for registration of medical devices for the Chinese market. All medical devices have to be classified by the CFDA according to its risk in three classes. Depending on the risk classification, different aspects are required: For medical devices of class I: product tests are sometimes required; For medical devices of class ...
An investigational device exemption (IDE) allows an investigational device (i.e. a device that is the subject of a clinical study [1]) to be used in order to collect safety and effectiveness data required to support a premarket approval (PMA) application or a premarket notification [510(k)] submission to Food and Drug Administration (FDA). [2]
Cabinet-level agencies are state and government institutions formed by the Constitutions and its subordinating laws whose roles and responsibilities are to support all government priorities and strategies set by the President.
Ministry of Interior and Administration - Arms Registration System (SRB) (non-searchable) - operated by the Policja and (in regard to private firearms of soldiers in active service) by the Military Gendarmerie; includes all firearms held by private persons, companies and public institutions, as well as their history, excluding the service ...
Single-use medical devices include any medical equipment, instrument or apparatus having the ability to only be used once in a hospital or clinic and then disposed. The Food and Drug Administration defines this as any device entitled by its manufacturer that it is intended use is for one single patient and one procedure only. [ 1 ]
The Audit Board of Indonesia (Indonesian: Badan Pemeriksa Keuangan) is the high state body responsible for checking the management and accountability of state finances conducted by the central government, local government, other state institutions such as Bank Indonesia, state-and municipally-owned enterprises, Public Service Boards, and ...