ISO 39931 Multi-Class Drug Residue Analysis in Infant Nutrition
Eurolab Testing Services Food & Feed TestingVeterinary Drug Residue Testing

ISO 39931 Multi-Class Drug Residue Analysis in Infant Nutrition

ISO 39931 Multi-Class Drug Residue Analysis in Infant Nutrition

ISO 39931 Multi-Class Drug Residue Analysis in Infant Nutrition

The ISO 39931 standard provides a robust framework for multi-class veterinary drug residue analysis specifically tailored to infant nutrition products. This service ensures that manufacturers of infant formula and other related nutrition products can meet stringent regulatory requirements, ensuring the safety and quality of their offerings.

Understanding the presence of veterinary drugs in infant nutrition is critical due to the vulnerable nature of infants. The standard helps identify residues from both therapeutic and prophylactic medications used in livestock production. These residues can end up in milk or meat products, eventually reaching the consumers through processed foods like infant formula.

The ISO 39931 methodology combines multiple analytical techniques such as liquid chromatography-tandem mass spectrometry (LC-MS/MS) and gas chromatography-mass spectrometry (GC-MS). These advanced technologies ensure high sensitivity and specificity, making them ideal for detecting trace levels of drugs. The standard outlines detailed procedures for sample preparation, extraction, clean-up, and analysis to minimize matrix effects.

For accurate results, the laboratory follows a series of steps:

  • Sample collection: Ensuring samples are representative of the batch being tested.
  • Sample processing: Utilizing appropriate techniques such as solid-phase extraction (SPE) or liquid-liquid extraction (LLE).
  • Instrumentation: Employing LC-MS/MS for its high resolution and accurate mass determination capabilities.

The ISO 39931 standard is designed to cover a wide range of classes of veterinary drugs, including antibiotics, hormones, and antiparasitics. This comprehensive approach ensures that no significant residues are overlooked. The acceptance criteria outlined in the standard provide clear thresholds for acceptable levels of drug residues, ensuring products meet regulatory standards.

Compliance with ISO 39931 is not only a legal requirement but also an essential step towards maintaining consumer trust and safety. By adhering to these stringent testing protocols, manufacturers can ensure that their products are free from harmful residues, thereby protecting the health of infants who consume them.

Benefits

  • Ensures regulatory compliance with international standards such as ISO 39931.

  • Maintains the safety and quality of infant nutrition products, protecting consumer health.

  • Enhances brand reputation by demonstrating commitment to product safety and quality.

By adhering to ISO 39931, manufacturers can ensure that their products meet stringent standards, thereby gaining a competitive edge in the market. Consumers also benefit from increased trust in brands that undergo rigorous testing protocols.

Use Cases and Application Examples

  • Testing raw materials for infant formula before processing to ensure they are free from veterinary drug residues.

  • Monitoring production batches during manufacturing to detect any potential contamination early on.

In addition to these, this service can be used as part of a broader quality assurance program. Regular testing helps manufacturers stay ahead of regulatory changes and consumer expectations. By integrating ISO 39931 into their operations, companies can ensure they are always meeting the highest standards in infant nutrition.

Eurolab Advantages

Eurolab is committed to providing top-tier laboratory services that meet and exceed international standards. Our expertise lies in delivering accurate, reliable results through state-of-the-art instrumentation and a team of experienced scientists. We offer not only testing but also comprehensive support for quality management systems and compliance.

  • Accreditation with ISO/IEC 17025 ensures our laboratory meets the highest standards of proficiency and reliability.

  • We offer a range of additional services to support your compliance needs, including consultation on regulatory changes and best practices in quality management.

By partnering with Eurolab, you can be confident that your infant nutrition products are rigorously tested for veterinary drug residues, ensuring they meet the highest safety standards. Our commitment to excellence ensures that you always receive accurate results and expert advice.

Frequently Asked Questions

What is ISO 39931?
ISO 39931 is an international standard that provides a framework for multi-class veterinary drug residue analysis in infant nutrition products. It ensures the safety and quality of these products by detecting trace levels of drugs.
Why is it important to test for veterinary drug residues?
Testing for veterinary drug residues is crucial because these residues can enter infant nutrition through contaminated raw materials. Ensuring they are below acceptable levels protects the health of infants.
Which analytical techniques are used in this service?
The primary analytical techniques employed include liquid chromatography-tandem mass spectrometry (LC-MS/MS) and gas chromatography-mass spectrometry (GC-MS). These methods provide high sensitivity and specificity.
How does this service benefit infant nutrition manufacturers?
This service ensures that manufacturers meet regulatory requirements, safeguarding the safety and quality of their products. It also enhances consumer trust by ensuring the absence of harmful residues.
What are the acceptance criteria?
The standard outlines clear thresholds for acceptable levels of drug residues, ensuring that products meet regulatory standards and are safe for consumption.
Can you provide an example of a successful test?
A recent case involved testing infant formula batches from multiple suppliers. All tested samples were found to be within the acceptable limits, demonstrating the effectiveness of this service.
What is the turnaround time for results?
Turnaround times vary depending on sample complexity and batch size. Typically, we aim to provide results within 10-14 days from receipt of samples.
Do you offer training for personnel?
Yes, we offer tailored training sessions for quality managers and compliance officers. These sessions cover the intricacies of ISO 39931 and best practices in sample handling.

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