From November 1st to November 4th, the CNCA organized an International Workshop on Good Laboratory Practice (hereinafter referred to as “GLPâ€) and a GLP Inspector Training Class in Beijing to further promote and strengthen the construction of a good laboratory standard monitoring system in China. Strengthen laboratory GLP capabilities.
At the seminar, Ms. Director of the Environment, Health and Safety Agency of the Organisation for Economic Co-operation and Development (OECD). Ms. Dian Turnheim presents the development trend of international GLPs in China and shares with non-OECD countries to join OECD/GLP
MAD's experience and discussions with Chinese authorities and experts on how China can participate more deeply in the work of the OECD Environment, Health and Safety Department.
It is understood that the OECD/GLP is a set of laboratory management rules and regulations prepared by the Organisation for Economic Co-operation and Development to ensure the high quality of safety chemical products, reliable test data, and mutual recognition of safety, while avoiding repeated tests for governments and The unnecessary waste caused by the company. GLP first originated in pharmaceutical research, and its concept was gradually extended to the laboratory safety evaluation of other toxic and hazardous substances, as well as the laboratory evaluation of various health-related products, and even included the management of most of the clinical laboratory testing. All laboratory research related to human health has now been covered. Data obtained from chemical tests conducted in accordance with the principles of OECD/GLP can be accepted by members of mutual recognition agreements and used as an evaluation basis for the protection of human health and environmental safety.
At the seminar, Ms. Director of the Environment, Health and Safety Agency of the Organisation for Economic Co-operation and Development (OECD). Ms. Dian Turnheim presents the development trend of international GLPs in China and shares with non-OECD countries to join OECD/GLP
MAD's experience and discussions with Chinese authorities and experts on how China can participate more deeply in the work of the OECD Environment, Health and Safety Department.
It is understood that the OECD/GLP is a set of laboratory management rules and regulations prepared by the Organisation for Economic Co-operation and Development to ensure the high quality of safety chemical products, reliable test data, and mutual recognition of safety, while avoiding repeated tests for governments and The unnecessary waste caused by the company. GLP first originated in pharmaceutical research, and its concept was gradually extended to the laboratory safety evaluation of other toxic and hazardous substances, as well as the laboratory evaluation of various health-related products, and even included the management of most of the clinical laboratory testing. All laboratory research related to human health has now been covered. Data obtained from chemical tests conducted in accordance with the principles of OECD/GLP can be accepted by members of mutual recognition agreements and used as an evaluation basis for the protection of human health and environmental safety.