Qmera Pharmaceuticals, Inc

Qmera Pharmaceuticals, Inc is listed as a small business research supplier in the Scientist.com network, with 2 sites in 1 country.

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Sites 2

Countries 1

Type of company: Small business

Chiral Separation Purify therapeutically active isomers of drug candidates.
High Resolution MS Elucidate the sequence and structure of peptides, proteins, biomarkers and organic compounds.
Ion Exchange Chromatography Separate and detect analytes.
Liquid Chromatography Separate substances using a mobile and stationary phase.
Non GLP Small Molecule Bioanalysis Detect and analyze the pharmacokinetic profile of small molecules.
Protein Binding HPLC Uses high pressure liquid chromatography to separate protein-drug complexes.

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Protein Separation and Detection Separate proteins based on properties such as solubility, adsorption or size differences.
Size Exclusion Chromatography Separate and identify analytes based on their molecular size.
Structural Elucidation Determine chemical structure of a compound. Characterization techniques include mass spectrometry, infrared spectroscopy and X-ray crystallography.

Drug Product Stability Use accelerated stress conditions to determine degradation pathways and identify manufacturing issues.
Forced Degradation Run light, heat, humidity, acid hydrolysis and oxidation tests to evaluate substance degradation.

LCMS Analysis Physically separate substances using liquid chromatography and mass spectrometry.
Method Development and Validation Develop and validate methods for synthesis and scale up of drug candidates.
USP Testing Analytical Reagents Acquire chemical reagents, solution concentrates and volumetric solutions used to evaluate items in USP testing.

LCMS/MS Analysis Liquid chromatography–mass spectrometry is an analytical chemistry technique that combines the physical separation capabilities of liquid chromatography with the mass analysis capabilities of mass spectrometry.
Quantitative MS Quantify small and large molecules in the pg/ml range

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Accelerated Stability Determine shelf life of drug formulations by comparing API breakdown at elevated temperature.

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