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  1. Purity method development for Ubrogepant and characterization of its degradation products
  2. Quantify the zinc content in zinc supplements employing HPLC/RID
  3. Ganirelix's secondary structure evaluation using Circular Dichroism Spectroscopy
  4. Applications of Fourier Transform Infrared and UV-Visible Spectroscopy for the demonstrating sameness of Ganirelix peptide in Liquid Injection Formulation
  5. Dehydrated alcohol (Ethanol) content in Clobetasol propionate foam by Gas chromatography
  6. Establishment of validated stability indicating purity method based on the stress degradation behavior of gonadotropin-releasing hormone antagonist (ganirelix) in an injectable formulation using HPLC and LC-MS-QTOF
  7. Temperature effect evaluation of the primary structure of Ganirelix using MALDI- TOF/TOF MS.
  8. Determination of Amino Acid Composition of Ganirelix Acetate in an Injectable Formulation by Pre-column Derivatization with 6-Aminoquinolyl-N-hydroxysuccinimidyl Carbamate
  9. ISOLATION, IDENTIFICATION, AND CHARACTERIZATION OF 17-OXO DEXAMETHASONE, AN OXIDATIVE DEGRADATION IMPURITY OF DEXAMETHASONE USING FLASH CHROMATOGRAPHY AND NMR/HRMS/IR
  10. DETERMINATION OF RESIDUAL CHLORIDE IN SEVELAMER CARBONATE USING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY