Moxidectin Residue Testing in Animal Feed
The use of veterinary drugs like moxidectin in animal feed is subject to strict regulatory controls aimed at ensuring food safety and public health. Moxidectin, a member of the avermectin family of anthelmintics, is widely used for the treatment or prevention of parasitic infections in livestock and companion animals. However, residues from these drugs can remain in animal tissues and products, potentially leading to contamination in animal feed if not properly managed.
Our service specializes in detecting moxidectin residues in animal feed samples using advanced analytical techniques that comply with international standards. This ensures compliance with regulatory requirements and provides peace of mind for quality managers, compliance officers, R&D engineers, and procurement teams involved in the production and distribution of animal feed.
The testing process begins with the collection of representative samples from various batches or sources within an animal feed facility. Proper sample preparation is critical to ensure accurate results. This involves homogenizing the feed material into a uniform mixture for analysis. Once prepared, the samples are analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS), which provides high sensitivity and selectivity needed for detecting moxidectin residues.
The acceptance criteria for this testing are stringent to ensure that no detectable residues exceed maximum residue limits (MRLs) set by regulatory bodies such as the European Food Safety Authority (EFSA), the World Health Organization (WHO), or other relevant agencies. These MRLs vary depending on the species of animal, tissue type, and intended use.
Our laboratory adheres to international standards including ISO/IEC 17025:2017 for quality management in testing and calibration laboratories. Compliance with these standards ensures that our results are reliable and can be trusted by all stakeholders involved in the feed industry.
| Applied Standards |
|---|
| ISO 17025:2017 |
| EFSA Guidance on the Determination of Veterinary Drug Residues in Foodstuffs |
| US FDA Guidance for Industry: Analytical Methods Validation |
Eurolab Advantages
- Pioneering expertise in veterinary drug residue testing.
- State-of-the-art LC-MS/MS equipment for accurate detection.
- Dedicated team of expert scientists and analysts.
- Comprehensive reporting tailored to your specific needs.
- Fast turnaround times without compromising accuracy or precision.
- ISO 17025:2017 accreditation ensuring reliability and validity.
Use Cases and Application Examples
Moxidectin residues in animal feed can arise from improper use of the drug or incomplete metabolism by animals. Our testing service is particularly useful for:
- Quality assurance programs aimed at maintaining product safety.
- Compliance checks conducted during routine inspections or audits.
- R&D projects focused on optimizing dosing regimens and minimizing residues.
- Investigations into incidents of suspected contamination in feed products.
