残留分析服务（RAS）

• 每年对大量不同种类的化合物进行残留分析，采用可靠、高效的24/7分析物定量法，使每年的高通量超过20000个样品
• 在方法开发、GLP方法验证和分析物定量方面拥有丰富的专业知识，以满足当前和新的监管要求
• 综合设施和高规格设备提供可靠可靠的数据

Your Needs

Identifying and characterizing residues in line with regulatory requirements and timelines

对于许多不同的监管评估，对于在作物中的残留量来评估与产品的运营商的风险来说，PPPS需要残留分析。这导致需要在各种研究中以符合，及时，具有成本效益和强大的方式产生高质量数据。在没有正确的洞察力和知识的情况下，驾驶如何有效地和战略方式进行具有挑战性。残留分析研究通常在PPP的监管之旅结束时进行，所以通过这些紧张的时间表，您需要快速的可靠数据。

我们的能力

Meeting all your residue analysis testing requirements quickly and cost effectively

As your partner, let us deliver all aspects of residue analysis testing for your PPP demanded by regulators across the globe. A cross-functional team of experts with extensive experience in residue analysis work tirelessly deliver the outcomes you require from single studies or whole work packages. The residue analysis service supports the following:

• 作物残留研究
• Crop processing studies
• 野外土壤消散研究
• 土壤累积研究
• 环境命运支持
• Ecotoxicology support
• Plant metabolism support
• Operator exposure studies

Facilities and staffing are designed to ensure a fast turnaround – most new method development projects are completed within 5 days.

由经验丰富的专门残留物分析团队管理的综合设施

我们的设施包括：

• Dedicated sample receipt and preparation area equipped to optimize sample preparation capacity and speed
• 专用样品提取和清理设施
• 操作人员暴露研究样品制备的移动分析支持
• 大型-20°C储存设施

分析方法现代化和创新适合您的具体需要

除了用于非复杂购买力平价的标准技术外，我们的团队还经常开发新的活性成分和代谢物分析方法。这意味着利用我们丰富的分析经验，修改现有的分析方法和利用最新的分析技术的见解。创新的例子包括：

• 开发新的提取程序
• Small-scale extraction methods for substances with limited matrix availability e.g. pollen
• ‘Scaling down’ equipment and reagents to enhance cost-effectiveness
• 利用QuEChERS方法和其他现有技术

Obviously, method validation is essential. Covance has the facility to perform independent laboratory validation for new methods from other laboratories and across our testing sites.

Leveraging high-specification equipment to delivery robust and reliably residue analysis data

With multiple instruments of varying specification available, we can flex our capacity to run samples 24/7 without sacrificing analysis quality. This optimizes sample throughput with >20,000 samples quantified each year and results provided to you in a timely manner. We have the full range of analytical equipment for active ingredient and metabolite quantitation, accuracy and reliability in line with GLP standards.