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Industrial Chemical Residue Analysis/
USP <621> Chromatography for Residue AnalysisUSP <621> Chromatography for Residue Analysis: Laboratory Testing Services Provided by Eurolab
Standard-Related Information
The United States Pharmacopeia (USP) <621> Chromatography for Residue Analysis is a laboratory testing service that ensures the quality and safety of pharmaceuticals, food products, and other materials. This standard is governed by various international and national standards organizations, including:
These standards dictate the requirements for laboratory testing services, ensuring that they meet specific quality control and assurance measures. The international and national standards that apply to this specific laboratory test include:
Standard Requirements and Needs
The USP <621> Chromatography for Residue Analysis testing service is required to ensure product safety, quality, and compliance with regulatory requirements. The need for this test arises from the risk of contamination with residues such as pesticides, heavy metals, or other substances that can have detrimental effects on human health.
The consequences of not performing this test include:
This testing service is essential for various industries, including:
Test Conditions and Methodology
The USP <621> Chromatography for Residue Analysis testing service involves the following steps:
1. Sample preparation: The sample is prepared according to specific guidelines, which may include extraction, purification, or concentration.
2. Instrumentation: High-performance liquid chromatography (HPLC) equipment is used to separate and detect the residues of interest.
3. Testing parameters: Specific testing parameters are applied, including temperature, flow rate, and detection limits.
4. Data analysis: The data collected from the HPLC instrument is analyzed using specialized software to identify and quantify the residues present in the sample.
The quality control measures during testing include:
Test Reporting and Documentation
The test results are documented and reported according to specific guidelines, including:
Why This Test Should Be Performed
The benefits of performing USP <621> Chromatography for Residue Analysis testing services include:
Why Eurolab Should Provide This Service
Eurolab has the expertise, experience, and resources to provide USP <621> Chromatography for Residue Analysis testing services. Our state-of-the-art equipment, qualified personnel, and accredited facilities ensure that our customers receive high-quality results.
Our laboratory is accredited by relevant standards organizations, including ISO 17025:2017 - General Requirements for the Competence of Testing and Calibration Laboratories. We have an international reputation for quality and reliability, with partnerships in over 100 countries worldwide.
Industry-Specific Examples and Case Studies
The following are examples of industries that require USP <621> Chromatography for Residue Analysis testing services:
Statistical Data and Research Findings
A study published in a reputable scientific journal demonstrated the importance of USP <621> Chromatography for Residue Analysis testing services:
Conclusion
USP <621> Chromatography for Residue Analysis is a critical laboratory testing service that ensures product safety, quality, and compliance with regulatory requirements. Eurolabs expertise, experience, and resources make us an ideal choice for this service. Our customers can trust our high-quality results, international reputation, and commitment to regulatory compliance.
References
1. USP <621> Chromatography for Residue Analysis
2. ISO 9001:2015 - Quality Management Systems
3. ASTM E2658-16 - Standard Guide for Establishing Consistency in the Measurement of Test Results
4. EN 45001:2009 - General Requirements for the Competence of Testing and Calibration Laboratories