Industry Applications
Industry Sector | Description of Application |
---|---|
Pharmaceuticals | To ensure drug purity and avoid contamination from residual solvents. |
Food & Beverage | Prevent contamination of food products during packaging. |
Cosmetics | Avoid adverse reactions due to trace amounts of harmful chemicals in finished products. |
Chemical Manufacturing | Ensure that final products meet strict quality and safety standards set by regulatory bodies. |
- Pharmaceutical manufacturers need to comply with USP , which sets limits for solvent residues in drug substances.
- Food & Beverage companies must adhere to FDA regulations regarding packaging materials used in contact with foodstuffs.
- Cosmetics firms should follow EU legislation on cosmetic ingredients and their safety profile.
- Chemical manufacturers have an obligation to test packaging according to ISO 15223:2016 for polyolefin films.
Eurolab Advantages
Eurolab offers comprehensive services tailored specifically towards packaging solvent residue testing. Our team of experts ensures that every aspect of your project—from sample preparation through final analysis—is conducted according to the highest standards. With years of experience and state-of-the-art equipment, we guarantee accurate results that are reliable and repeatable. Our commitment extends beyond just performing tests; our consultants provide valuable insights into interpreting results and offering recommendations for improvements where necessary. Whether you're dealing with a one-off project or an ongoing program, Eurolab is here to support your needs comprehensively.Quality and Reliability Assurance
At Eurolab, we understand the importance of quality assurance in ensuring consistent and dependable results from our tests. Our approach combines advanced technology with meticulous attention to detail at every stage of the process.- We use gas chromatography equipped with flame ionization detectors (GC-FID) for precise quantification.
- Our laboratories are certified to ISO/IEC 17025, ensuring compliance with international standards.
Frequently Asked Questions
Why is it important to test for solvent residues in packaging?
Testing for solvent residues is crucial because even trace amounts can pose significant risks. These residues might migrate into the product, affecting its quality and safety. Compliance with international standards like ISO 15223:2016 helps ensure that packaging materials meet strict purity requirements.
Can you perform this testing on any type of packaging material?
Yes, we can analyze a wide range of materials including plastics, paperboard, laminates, and more. Our expertise ensures that no matter what kind of packaging is involved, the right methodology will be applied.
How long does it take to complete a solvent residue test?
Typically, results can be delivered within 7-14 business days from receipt of sample. However, this timeline may vary slightly based on the complexity of the analysis.
What happens if residues are found in excess?
Excessive solvent residues indicate potential contamination issues which must be addressed immediately. Our team will work closely with you to investigate further and provide solutions to mitigate risks.
Do you offer custom testing packages for unique packaging types?
Absolutely! We recognize that every client has different needs, so we tailor our services accordingly. Let us know about your specific requirements and let's discuss how best to serve them.
What certifications do you hold related to this service?
Eurolab holds ISO/IEC 17025 accreditation, ensuring our tests meet international standards. This certification guarantees the accuracy and reliability of all results produced in our laboratories.
Can you provide test reports for regulatory submissions?
Certainly! Our detailed reports include comprehensive information suitable for both internal documentation and external submissions to authorities. These documents are designed to meet the highest standards of transparency and accuracy.
How does Eurolab ensure consistent test results?
We achieve consistency through rigorous quality control measures, including regular instrument calibration and proficiency testing against recognized reference materials. This ensures that all tests are conducted accurately and consistently.