The Pharmaceutical Affairs Law subjects pharmaceuticals, quasi-drugs, and medical devices to various approval and permit systems, such as licence for marketing ...

Pharmaceutical administration in Japan is based on various laws and regulations, consisting mainly of: (1) Pharmaceutical and Medical Device Act, (2) Law.

11 мар. 2024 г. · The Pharmaceuticals and Medical Devices Act is a law that regulates necessary aspects such as manufacturing, labeling, sales, distribution, and advertising of ...

Japanese. Pharmaceuticals and Medical Devices. Policy Information. Outline of the Law for Partial Revision of the Pharmaceutical Affairs Law (Act No.84 of 2013) ...

Japan's Pharmaceutical Affairs Law (PAL) establishes regulations covering the manufacturing and distribution of medical devices and pharmaceutical products in ...

Article 15-12(1)A pharmacy proprietor must have a pharmacist engaged in sales or provision of medicines at a pharmacy provide information or instruction under ...

The title of the Pharmaceutical Affairs Law is revised to the “The Law on Securing Quality, Efficacy and Safety of Products including. Pharmaceuticals and ...

JPAL stands for Japanese Pharmaceutical Affair's Law. The JPAL establishes regulations covering the manufacturing and distribution of medical devices and ...

The PMD Act provides the legal framework for the regulation of medical devices, in vitro diagnostic reagents, pharmaceuticals, drugs and cosmetic products.

The purpose of this Act is to improve health and hygiene by providing the control required for securing the quality, efficacy and safety of pharmaceuticals.