A lot of questions are still raised by the decision of the EEC Board adopted in February 2018 “On residues of veterinary medicinal products”. Find out about the challenges the industry is facing, as well as the views of market participants on amending existing standards regarding antibiotics, in The DairyNews.
As you know, today more than 70 types of antibiotics are used in animal husbandry. Technical regulation TS 021/2011 "On food safety" regulates the use of six groups of veterinary drugs in products of animal origin - levomycetin, tetracycline group, streptomycin, penicillin for Milk. In the case of Meat, poultry, eggs, fish and other products, the presence of grizin and bacitracin is checked.
Meanwhile, according to the 28th decision of the EEC Board, which entered into force in the summer of 2018, IT is entrusted to manufacturers, suppliers, as well as during production control and control by supervisory authorities, to control antibiotic residues in raw materials and products of animal origin. According to the EEC clarification, the list of the Decision does not oblige to carry out production control for the presence of all veterinary medicinal products included in it. At the same time, entrepreneurs are given the opportunity to implement a risk-based approach. This means that when purchasing raw materials, such as meat, receiving information from the supplier about the antibiotics used, the processor, if he deems it necessary, can check the products for the presence of residues of these particular antibiotics. At the same time, the document gives the right to entrepreneurs to use any research methods, which greatly simplifies their work. The players call the main problem the expensive methods described in the document.
The problem of regulations in the country is not only characteristic of the issue of determining drugs in milk. However, this topic remains relevant for the industry.
According to Yulia Eliseeva, Director of technical regulation at Danone in Russia, there are more than 30 standards for determining the residual amount of antibiotics in dairy products in the country. These standards, according to her, need to be combined into one GOST for all products. Here is how the expert argued this position:
“It is known that there are quantitative and qualitative methods for controlling the content of antibiotics in dairy products. The problem is that we do not have a unified methodology, a unified approach to qualitative methods. Each method uses its own device, each has its own sensitivity limit. As a result, we have a huge range of methods that are not comparable with each other. Maybe we should review all the methods and make one GOST? - suggested Yulia Eliseeva.
Danone's position has been criticized by representatives of the dairy industry. In particular, Elena Yurova, Head of the VNIMI technochemical control laboratory, in an interview with The DairyNews noted that each of the existing standards is a different document in its essence:
“The existing thirty-two standards for the determination of antibiotics and veterinary drugs are different documents, each of which standardizes method for determining a particular substance. There can be many more of them, and there is nothing wrong with that, everyone can use what they want, - said Elena Yurova. "The proposal to merge all the standards seems to be moving forward with the goal of not allowing standards for screening methods."
Just screening methods, according to Elena Yurova, are the most effective in determining the residual amount of drugs in dairy products. They are used in all countries of the world, including laboratories of regulatory organizations.
“ELISA or screening methods are the fastest and easiest way to detect different drugs at the same time in one sample when we don't know which drugs were used on the farm. Using enzyme immunoassay, we can detect up to 128 substances in one sample. That is why these methods are widely used all over the world,” said Elena Yurova.
The expert noted the following problems in the determination of antibiotics in dairy products:
- The introduction of antibiotics into raw milk as a form of falsification. Medicines can be added directly to milk, as well as enter the milk through the body of the animal.
- A single rationing of antibiotics in the amount of 0.01 mg/kg of the tetracycline group is not taken into account when accepting raw milk. Companies may not consider that when making products containing concentrated milk solids (cheese, cottage cheese, products produced by nanofiltration), the content of antibiotics increases with an increase in the proportion of milk.
“The product at the end may turn out with an overestimated share of antibiotics. This once again proves that the control of antibiotics and veterinary drugs needs to be improved, since according to the law, the entire production process must be transparent,” said Elena Yurova.
Who should monitor medicines in milk?