As a contract research organisation with state-of-the-art laboratory equipment, we offer expertise and consulting services for your specific projects.
We develop, validate and support the implementation of analytical methods and interpret analytical data in support of drug substance (API), pharmaceutical dosage forms (DP) and stability from early development to commercialisation.
Our expertise includes:
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- Pharmaceutical development: Analytical support to preformulation, formulation, API, excipients, impurities, degradation products.
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- Analytical techniques: HPLC, UHPLC, LC-MS, LC-MS/MS, UV-VIS.
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- Development and validation of bioanalytical chromatographic methods for quantification of active substances and their metabolites in various biological matrices
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- Stability testing, development, validation and transfer of stability indicating methods
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- Validation of analytical methods
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- Clinical trials consulting
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- Quality Assurance: Quality by Design (QbD)
Our services are tailored to your needs to help your business improve its efficiency, implement new strategies and ensure its growth.
For more information Contact us.