We specialize in Method Development, Validation, and Transfer in alignment with pharmacopoeial monographs and regulatory guidelines (ICH, USP, EP, BP, etc.).

Our expert scientists design and optimize analytical methods to ensure accuracy, precision, specificity, and robustness, tailored to your product profile. We offer:

• Method Development for monograph and non-monograph products
• Method Validation following ICH Q2(R1) guidelines
• Analytical Method Transfers with complete documentation and technical support

With a commitment to compliance, quality, and reliability, we ensure smooth method lifecycle management—from initial development through to regulatory acceptance and routine QC use.