Publish Time: 2022-03-17 Origin: Site
Veterinary drugs, also known as animal drugs, refer to livestock and poultry drugs in a narrow sense, and drugs that prevent and treat all animal diseases except humans and promote their growth and reproduction in a broad sense. Veterinary drugs and human drugs promote each other and develop synchronously in research and development. So what is the regulatory pathway for veterinary drugs residues? Let's take a look.
Here is the table of contents:
l Improve laws and regulations
l Standardize production use
To reduce the residual problem of veterinary drugs, effective regulatory measures should be taken. First of all, it is necessary to do a good job of perfecting legal norms and make clear norms and requirements for veterinary powder residues to ensure that the monitoring of veterinary powder residues has laws to abide by. A comprehensive and complete "Food Safety Law" should be formulated to strictly regulate the safety indicators of food, and strict penalties should be imposed on behaviors that violate the law. Fully implement and implement the "Regulations on the Administration of Veterinary Drugs", "Regulations on the Administration of Feed and Feed Additives", "The Maximum Residues of Veterinary Drugs in Animal Foods" and other normative requirements. A sound veterinary external medicine operation, management and distribution system should be built, and counterfeit and low-quality medicines should be strictly checked and cracked down. According to the standard requirements, strictly test the content of amino acids, vitamins, trace elements, and other elements in the feed to ensure that each element is within the index range required by the standard. It is necessary to establish, improve and revise the standards for the use of various drugs, strictly implement the withdrawal period system, and strengthen supervision and management from various aspects.
To ensure the effectiveness of Veterinary Drugs residue supervision, we should start from the source, strictly supervise and manage veterinary drug manufacturers, ensure that the production of veterinary tablets meets the standard requirements, and prevent veterinary tablets with unknown ingredients and labels from entering the market. Strictly investigate and deal with illegal drugs. The monitoring of feed production should be done well, and the use of feed with additives should be avoided. During the breeding process, we must also do a good job in the use of veterinary powder, strictly abide by the withdrawal period, strengthen education and publicity and other work, improve the safety awareness of the breeding staff, and enable them to master the scientific method of drug use. According to the "Veterinary Drug Administration Regulations", the "Veterinary Drug Production Quality Management Specification" should be formulated to manage and control the production of Veterinary Drugs, and make clear requirements and specifications to reduce the risks of contamination, cross-contamination, confusion, and errors in the production process of veterinary drugs, ensuring veterinary external medicine.
The production quality meets the standard requirements. It is necessary to implement the standard requirements of veterinary drug production, control, storage, and sales, determine the existing quality objectives, and personnel at different levels must assume different responsibilities. At the same time, improve the relevant facilities and equipment to ensure that the quality objectives can be effectively met. Production enterprises should establish a sound quality assurance system and document system to ensure the effectiveness of the system operation.
The above is the relevant content about the regulatory path of veterinary drugs residues. If you are interested in veterinary drugs, veterinary external medicine, veterinary oral solutions, you can contact us.