Measures for supervision and inspection on veterinary drug clinical and non-clinical research quality management standards.
Country
Type of law
Regulation
Abstract
The purpose of these Measures is to strengthen and standardize the supervision and inspection on veterinary drug good clinical practice (GCP) and veterinary drug good laboratory practice (GLP), and to improve the scientificity and accuracy of veterinary drug research and test evaluation data.
The Ministry of Agriculture shall be responsible for formulating technical specifications and guidelines for veterinary drug GCP and veterinary drug GLP supervision and inspection, and organizing the implementation of supervision and inspection of veterinary drug safety evaluation units. The Working Committee for the Management of Veterinary Drugs Quality Standards and Specifications shall be established by the Ministry of Agriculture.
The Ministry of Agriculture shall be responsible for formulating technical specifications and guidelines for veterinary drug GCP and veterinary drug GLP supervision and inspection, and organizing the implementation of supervision and inspection of veterinary drug safety evaluation units. The Working Committee for the Management of Veterinary Drugs Quality Standards and Specifications shall be established by the Ministry of Agriculture.
Attached files
Web site
Date of text
Repealed
No
Source language
English
Legislation Amendment
No
Original title
兽药临床与非临床研究质量管理规范监督检查办法.