Method Development & Validation
Aptiance has world class experts in the pharma-research and analyticals for conducting high-quality, time and cost effective method development and validation services for any molecular entities, active pharmaceutical products, drugs, excipients or clinical trial samples. Currently we offer non-GLP Assays.
Our state-of-the-art instruments' capabilities include:
Aptiance has world class experts in the pharma-research and analyticals for conducting high-quality, time and cost effective method development and validation services for any molecular entities, active pharmaceutical products, drugs, excipients or clinical trial samples. Currently we offer non-GLP Assays.
Our state-of-the-art instruments' 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
- Protocol consultation and suggestion.
- Method remediation.
- Sample preparation (solid Phase, liquid phase).
- Robust and reliable Method Development and validation for any molecular entity.
- Analytical methods Transfer to any laboratory.
- Preformulation and postformulation studies to establish active ingredient composition.
- Analysis to establish Quality and purity.
- and testing (USP-NF, EP, BP) for active ingredients and excipients.
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