POTENCY
ANALYSIS
Quantitative HPLC analysis against certified reference standards using validated HPLC methods. Accurate concentration and potency determination using multi-point calibration curves for peptides, APIs, and research compounds.
- 01Active ingredient quantification
- 02Concentration determination
- 03Content uniformity testing
- 04Dose verification
- 05Raw material assay
Potency analysis at Standard Analytica determines the exact concentration of your active compound using external standard quantification. A multi-point calibration curve is prepared from certified reference standards to ensure accuracy.
This method is essential for dose verification, content uniformity testing, and raw material assay. Results are reported as mg/mL, mg/g, or percent label claim depending on your requirements.
All quantitative methods are validated for linearity, accuracy, precision, and range in accordance with ICH Q2(R1) guidelines.
SAMPLE INTAKE
Your sample is received, logged into our LIMS system, and assigned a unique tracking identifier. Sample integrity is verified and documented upon receipt.
PREPARATION
Samples and certified reference standards are weighed and prepared according to validated protocols. Multi-point calibration solutions are prepared from the reference standard.
ANALYSIS
Calibration standards and samples are injected into our HPLC system. A calibration curve is established, and sample concentration is determined by interpolation.
REPORTING
Results including calibration curve, linearity data, concentration values, and recovery calculations are compiled into a comprehensive report with full chromatographic data.
SUBMIT A SAMPLE
Ready to submit a sample for potency analysis? Order online or contact our team to discuss your requirements.