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To better assist you with your request, please choose a research area provided by Eurofins CDMO Alphora Inc. In case you cannot find an exact match, simply select any service, and our concierge team will swiftly address it once your request has been submitted.

Solubility Studies

Analyze substances for kinetics of solubility using nephelometry and UV-Vis spectrometry.
Chemistry, Manufacturing and Controls (CMC)

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Method Development and Validation

Develop and validate methods for synthesis and scale up of drug candidates.
Chemical Stability

Measure the stability of small molecules in solution.
NMR Structure

Determine molecular structure, identify chemical impurities and validate sample integrity.
Impurity Synthesis

Use high resolution MS or NMR to eliminate intermediates or organic byproducts and determine impurity content.
High Resolution MS

Elucidate the sequence and structure of peptides, proteins, biomarkers and organic compounds.
GMP Synthesis

Synthesize APIs including small molecules, formulations and protein-based drugs under GMP compliance.
Analytical Development and Validation

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Thermal Analysis

Characterize compounds based on calorimetry and thermodynamic data.
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