Precision
Analytical
Science.
Specialized analytical and research services for pharmaceuticals and medical devices. LC-MS/MS, ICP-MS, and cutting-edge technology for regulatory compliance.
Trusted by Industry Leaders
Global Quality Accreditations
Our facility operates under strict international guidelines to ensure regulatory-ready data.
Industries We Serve
Our expertise lies in conducting both qualitative and quantitative study and analysis.
Pharmaceutical Industries
Ensuring safety and efficacy with advanced analytical testing, extractables & leachables, and method validation.
Pharmaceutical Packaging
Evaluating primary and secondary packaging materials to ensure they are safe and compliant for drug storage.
Medical Devices
Rigorous extractables and leachables testing to guarantee medical device safety and regulatory compliance.
Our Core Services
Industry-leading analytical solutions engineered for pharmaceutical innovation and strict regulatory compliance.
Why Choose Us
Why Pharmaceutical Companies Trust CLS
Frequently Asked Questions
Our standard turnaround time is 10-15 business days depending on the complexity of the method and the volume of samples. We also offer expedited services for critical path projects.
Yes, all our analytical reports are fully validated, QA-reviewed, and formatted to meet the strict submission requirements of the FDA, EMA, CDSCO, and other global regulatory bodies.
Absolutely. We operate under strict Non-Disclosure Agreements (NDAs) and employ robust data integrity protocols to ensure your intellectual property is completely secure at all times.
Sample size requirements vary depending on the specific analytical method and the matrix involved. Our scientific team will provide precise requirements during the initial consultation phase.
Our laboratory is NABL Accredited (ISO/IEC 17025:2017), ISO 9001:2015 certified, CDSCO approved, and fully compliant with FDA 21 CFR Part 11 requirements for electronic records.
Need Analytical Testing?
Talk to our experts today to discuss your project requirements and timelines.