At the same time, check whether the packaging seal is complete and damaged; Check whether there is a use period and production batch number, and veterinary drugs should be used within the use period; Visually inspect veterinary drugs to see if there is any abnormality. Water agent to see if discoloration, precipitation, crystallization, turbidity, mildew and so on. ; Powder to see if it absorbs moisture, mildew, discoloration, etc. ; Check whether the flat plate is wet, discolored, deformed and moldy. ; Powder injection to see if it changes color, deliquescence, caking, mildew, etc. ; Tincture, emulsion to see if there is stratification, precipitation, odor, etc.
Specific query method:
1, go to a reliable website.
At present, the network information is huge, and all kinds of information are flooded, so it is difficult to distinguish between true and false. Being good at using the public information of government websites for identification is one of the most reliable methods. Government websites have special public information for public inquiry and verification. The domain name suffix of China government website is ". The website with this suffix is a trusted website.
To distinguish the authenticity of the veterinary drug product number, you can query the "China Veterinary Drug Information Network" (website:) "Veterinary drug basic information query system". The information that can be inquired by this system includes: the approval number data of veterinary drug products and the registration data of imported veterinary drugs, the batch issuance data of veterinary biological products, and the results of veterinary drug supervision and sampling inspection.
2. Check the nature of the website of the production or distribution unit.
First of all, you can query the information of the website in the "Domain Name Information Filing Management System" (website:). Including: the name, nature and website name of the organizer, the name of the person in charge of the website, the website filing/license number, and the domain name.
Secondly, it can help the "National Enterprise Credit Information Publicity System" (website:) to query the information of enterprises, farmers' professional cooperatives and individual industrial and commercial households, and all legal units can find it, otherwise it will be illegal.
Finally, to distinguish between genuine and fake websites, these websites have several characteristics: they use overseas servers, have no domain name information record number or steal others' record number, and the certificate pictures displayed on the webpage are vague and unrecognizable. If you have one of these items, you should be vigilant and use the first few points to verify.
3. Be good at distinguishing the authenticity of magazine advertisements.
Advertisements related to drugs published in standard journals will have the Guang Shen symbol (veterinary drug advertisement approval symbol), which is approved by the competent agricultural department to ensure that the published veterinary drugs are the true information of the regular products of regular manufacturers.
4. Veterinary drug QR code
From 20 16 65438+ 10/0/,China will start the retrospective management of veterinary drug management in an all-round way, and veterinary drugs can be scanned and queried.
I hope the above content can help you. If in doubt, please consult a professional lawyer.
Legal basis:
Article 6 of the Regulations on the Administration of Veterinary Drugs
The state encourages the development of new veterinary drugs and protects the legitimate rights and interests of developers according to law.
Article 7
To develop a new veterinary drug, it is necessary to have a place, equipment, professional and technical personnel, safety management norms and measures suitable for the development.
Safety evaluation should be carried out in the development of new veterinary drugs. Units engaged in the safety evaluation of veterinary drugs shall be approved by the veterinary administrative department of the State Council, and shall abide by the quality management standards for non-clinical research of veterinary drugs and the quality management standards for clinical trials of veterinary drugs.
Article 8
The development of new veterinary drugs shall be filed with the veterinary administrative department of the people's government of the province, autonomous region or municipality directly under the Central Government where the clinical trial site is located before the clinical trial, and the pre-clinical research data such as the safety evaluation report of the new veterinary drugs in the laboratory stage shall be attached.
If the new veterinary drug developed belongs to biological products, it shall apply to the veterinary administrative department of the State Council before the clinical trial, and the veterinary administrative department of the State Council shall notify the applicant in writing of the evaluation results within 60 working days from the date of receiving the application.
If the development of new veterinary drugs requires the use of a class of pathogenic microorganisms, it shall also meet the conditions stipulated by the veterinary administrative department of the State Council, and report to the veterinary administrative department of the State Council for approval before the laboratory stage.