EN 22599 Antiparasitic Residue Profiling in Infant Foods
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EN 22599 Antiparasitic Residue Profiling in Infant Foods

EN 22599 Antiparasitic Residue Profiling in Infant Foods

EN 22599 Antiparasitic Residue Profiling in Infant Foods

The European Standard EN 22599 specifies a method for determining antiparasitic drug residues in infant foods. This standard is critical for ensuring the safety of infants and young children by preventing exposure to potentially harmful levels of antiparasitic drugs that may have been inadvertently introduced during food production, processing, or storage.

The antiparasitics used in livestock are designed to be metabolized quickly after slaughter, but trace amounts can remain in meat, milk, and other animal products. These residues can enter the infant diet through various forms of processed foods such as baby cereals, baby formulas, and other infant-specific meals. The presence of even low levels of antiparasitic drugs in infant foods can pose significant health risks to infants due to their developing organ systems.

EN 22599 provides a robust framework for laboratories to follow when testing for these residues. This method involves the extraction of the sample, cleanup procedures to remove interfering substances, and subsequent analysis using validated analytical techniques such as high-performance liquid chromatography (HPLC) or gas chromatography-mass spectrometry (GC-MS).

The standard outlines specific steps for sample preparation, including homogenization and extraction processes that are designed to ensure the accurate quantification of antiparasitic residues. The method also specifies limits of detection and quantitation, which are crucial for determining whether residue levels exceed acceptable thresholds.

For infant foods, the permissible limits for antiparasitic drug residues are set by regulatory bodies such as the European Food Safety Authority (EFSA). Laboratories must adhere to these guidelines when interpreting test results. Compliance with EN 22599 is not only important from a legal standpoint but also enhances consumer confidence in the safety of infant foods.

Understanding and adhering to this standard helps food manufacturers ensure that their products meet stringent quality control standards, thereby protecting public health. The method is particularly relevant for companies involved in the production of baby formulas or other processed infant foods as it ensures that these products do not contain unsafe levels of antiparasitic drugs.

Compliance with EN 22599 also provides a competitive advantage by ensuring that food manufacturers can demonstrate their commitment to safety and quality. This is especially important in an increasingly regulatory-driven market where consumers are more informed about the safety of the products they purchase for their children.

Environmental and Sustainability Contributions

  • Informed Decision Making: By ensuring that infant foods do not contain harmful levels of antiparasitics, this standard contributes to a healthier environment by reducing the risk of adverse health impacts on infants.
  • Eco-friendly Operations: Compliant laboratories play a crucial role in maintaining a sustainable supply chain. Their meticulous testing ensures that only safe and high-quality ingredients are used in infant foods.

Competitive Advantage and Market Impact

  1. Consumer Trust: Compliance with EN 22599 builds trust among consumers, who can feel confident that the products they purchase for their children meet stringent safety standards.
  2. Maintaining Reputation: In an industry where reputation is paramount, adhering to this standard helps maintain a company’s integrity and reputation in the market.

Frequently Asked Questions

What specific antiparasitic drugs are tested under EN 22599?
EN 22599 covers a range of commonly used antiparasitics in livestock, including levamisole, pyrantel pamoate, and fenbendazole. The standard is designed to detect these drugs at trace levels that may be present in infant foods.
What are the consequences of failing to comply with EN 22599?
Failing to comply can result in legal penalties, loss of market share, and damage to a company’s reputation. Non-compliance may also lead to product recalls, which can be costly and damaging.
How often should laboratories perform this test?
The frequency of testing depends on the manufacturing process and supply chain. Laboratories typically recommend regular testing as part of routine quality control checks, especially for products with a high risk of contamination.
What is the role of laboratories in ensuring compliance?
Laboratories play a crucial role by providing accurate and reliable test results. They must ensure that their methods are validated against EN 22599 standards to provide consistent and repeatable results.
Is this method applicable only to infant foods?
No, while the standard is specifically designed for infant foods, its principles can be applied to other processed animal-based food products as well. The key is ensuring that all processed foods are free from harmful residues.
How does this method differ from other residue testing standards?
EN 22599 focuses specifically on antiparasitic drugs and their residues in infant foods. Other standards may cover a broader range of drug types or different food categories.
What role do international standards play?
International standards like EN 22599 provide harmonization across borders, ensuring consistency in residue testing practices and results. This is particularly important for global supply chains.
What are the implications of not adhering to this standard?
Not adhering to EN 22599 can lead to health risks, legal action from regulatory bodies, and reputational damage. It also undermines consumer trust in the product.

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