Analytical-Bioanalytical
Aptiance offers Analytical-Bioanalytical support services for research, drug development and biotechnology needs for method transfer, development, validation and analysis of non-clinical, preclinical and clinical biological samples currently in a non-GLP setting. Our state-of-the-art instruments’ capabilities, expert opinions and quality services enhance your productivity and help to ensure consistent, reliable support.
Aptiance offers personalized support with an emphasis on quality, accuracy and speed. Our mission is to provide the best possible quality and service at competitive prices. Currently we offer non-GLP Assays only.
Our Capabilities include:
Aptiance offers Analytical-Bioanalytical support services for research, drug development and biotechnology needs for method transfer, development, validation and analysis of non-clinical, preclinical and clinical biological samples currently in a non-GLP setting. Our state-of-the-art instruments’ capabilities, expert opinions and quality services enhance your productivity and help to ensure consistent, reliable support.
Aptiance offers personalized support with an emphasis on quality, accuracy and speed. Our mission is to provide the best possible quality and service at competitive prices. Currently we offer non-GLP Assays only.
Our Capabilities include:
- LC-MS, LC-MS/MS, LC-MS-QTOF, (qualitative and quantitative)
- HPLC with diode array UV/VIS, and fluorescence detection
- Automated sample processing and analysis
- Chemical synthesis of standards.
- Organic Synthesis in miligram to gram scale.
- Semi Prep-LC for analytical compound purification in micro to milligram scale
- Chromatography, chemical sample or any biological matrix analysis
- Method development, method transfer, modify existing method
- Metabolic studies, profiling, identification, prodrug conversion characterization using multiple analytical platforms
- Quality assurance, purity determination, impurities identification, isolation
- Proteins and peptides identification study
- Quantitative analysis of peptides and small molecules identified as novel biomarkers
- Formulation support, dose formulation analysis, quality assurance, method development, validation
- Steroids and drugs of abuse analysis, detection in low concentration
- Steroids metabolism detection, identification, quantitation
- Pharmaceutical testing in environment using EPA methods
- Non-clinical substance analysis, method development and results interpretation
- Technology consultation/support
- Implementation and validation of LC/MS, LC/MS/MS Q-TOF methodology.
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