SCIENTIFIC LABORATORY VERTICALS
Analytical and Pharmaceutical Research
Complete protocol details, validated deliverables, and regulatory compliance standards.
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Category: Analytical
Technical Parameters
Advanced testing, chromatography fingerprinting, and structural characterization for active pharmaceutical ingredients and formulations.
Technical SOP Protocols
- Qualitative & Quantitative HPLC Analysis under GMP/GLP standards.
- High-Performance Thin-Layer Chromatography (HPTLC) fingerprinting.
- Bio-analytical testing (plasma, serum, and tissue distribution profiles).
- Advanced Spectral Analysis: 1D/2D H-NMR, C13-NMR, MASS, LC-MS, IR spectroscopy.
- Thermal Analysis: Differential Scanning Calorimetry (DSC) and Thermogravimetric Analysis (TGA).
- Structural and Surface Characterization: XRD, SEM, Zeta Potential, and AAS.
- Disintegration & dissolution studies for generic and proprietary solid dosages.
Select Laboratory Plan
Standard Level
Deliverables Included
- Qualitative HPLC assay reports
- Single-wave UV spectrum files
- Basic dissolution profiling
- Turnaround: 12-14 business days
Premium Validation Tier
Expanded Scope
- Full quantitative validation study under ICH guidelines
- Detailed spectral deconvolution (1H-NMR, 13C-NMR, LC-MS overlay)
- High-resolution SEM microphotographs with particle-size distribution curves
- Zeta potential & XRD mineralogical profiling
- Regulatory compliance-ready certificate of analysis (CoA)
- Turnaround: 5-7 business days
Request Protocol Booking
Specify your research coordinates to trigger an NDA & feasibility evaluation.