ISO 65691 Multi-Class Drug Testing in Dairy Powders
Eurolab Testing Services Food & Feed TestingVeterinary Drug Residue Testing

ISO 65691 Multi-Class Drug Testing in Dairy Powders

ISO 65691 Multi-Class Drug Testing in Dairy Powders

ISO 65691 Multi-Class Drug Testing in Dairy Powders

The ISO 65691 standard provides a robust framework for detecting multi-class veterinary drug residues in dairy powders. This service is critical for ensuring compliance with international food safety standards, particularly when sourcing raw materials from various suppliers or countries.

Dairy powder manufacturers and processors need to be certain that their products meet stringent quality and regulatory requirements. The presence of even trace amounts of illegal or sub-therapeutic veterinary drugs can compromise product integrity and lead to potential health risks for consumers.

Our laboratory uses cutting-edge analytical techniques, including high-performance liquid chromatography (HPLC), mass spectrometry (MS/MS), and gas chromatography-mass spectrometry (GC-MS) to identify over 100 different classes of veterinary drugs. These tests are performed in accordance with the ISO 65691 standard, ensuring accuracy and consistency.

Sample preparation is a critical step that involves thorough extraction methods tailored to the matrix of dairy powders. This process ensures complete dissolution of potential residues without affecting test results. After extraction, samples undergo analysis by our state-of-the-art instruments, which provide precise quantification levels down to parts per billion.

Our team of experts can tailor testing protocols based on specific client needs or regional regulations. Whether you require routine testing for a single batch or comprehensive quality control measures over an entire production run, we offer flexible solutions that fit your business requirements.

Use Cases and Application Examples
Scenario Description
Dairy Powder Manufacturer Compliance Testing batches to ensure compliance with international standards.
R&D Innovation Exploring new methods for minimizing drug residues in dairy powders.
Purchase Verification Evaluating incoming raw material shipments from different suppliers.

Eurolab Advantages

  • State-of-the-art instrumentation and skilled personnel ensuring precision.
  • Comprehensive knowledge of international standards like ISO 65691 for accurate testing.
  • Predictive analytics to forecast potential issues before they arise.
  • Customized solutions meeting specific client demands or regional regulations.

We pride ourselves on delivering reliable results quickly and efficiently, enabling our clients to make informed decisions promptly. Our commitment to excellence is reflected in every aspect of the testing process—from initial consultation through final report generation.

Quality and Reliability Assurance

  1. Our laboratory adheres strictly to ISO 65691 guidelines, ensuring all tests are conducted under controlled conditions.
  2. We employ rigorous quality control measures at every stage of the testing process.
  3. Trained personnel ensure consistency and accuracy in sample preparation and analysis.

The reliability of our results is further enhanced by regular calibration of instruments, participation in proficiency testing programs, and continuous training for staff. These practices guarantee that our clients receive accurate and trustworthy data they can rely on when making important business decisions.

Use Cases and Application Examples

  • Dairy Powder Manufacturer Compliance: Testing batches to ensure compliance with international standards.
  • R&D Innovation: Exploring new methods for minimizing drug residues in dairy powders.
  • Purchase Verification: Evaluating incoming raw material shipments from different suppliers.

Our expertise extends beyond just detection; we also offer advice on best practices to reduce the presence of veterinary drugs in your product. By understanding where these residues come from and how they affect quality, you can implement strategies that lead to better outcomes across all stages of production.

Frequently Asked Questions

How long does it take to complete a full round of testing?
Typically, we can provide preliminary results within 5 working days and final reports within 10 working days. However, this may vary depending on the complexity of the sample.
What kind of equipment do you use for these tests?
We utilize advanced analytical techniques such as HPLC, MS/MS, and GC-MS to ensure precise quantification levels down to parts per billion.
Can you test specific types of drugs?
Yes, we can target specific classes of veterinary drugs as required by our clients. This flexibility allows us to cater to diverse needs within the industry.
How do you handle confidential information?
We maintain strict confidentiality protocols, ensuring all data remains secure and is only accessible by authorized personnel.
What if I have more than one batch to test?
Our team can prioritize your samples based on urgency or frequency, ensuring timely service without compromising quality.
Do you offer training sessions for our staff?
Absolutely! We provide educational workshops and seminars to help your team understand the latest testing methods and best practices.
What kind of support do you offer post-testing?
We offer detailed reports along with recommendations on how to address any issues identified during testing, ensuring continuous improvement in your operations.

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our expert team is ready to guide you every step of the way.

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