Invitron Advanced Analytics

INVITRON Advanced Analytics is a full-fledged c-GLP compliant, analytical laboratory that provides full range of testing services for products targeting global market. We are based in Hyderabad, India, with a state-of-the-art testing facility of sq ft with most advanced instruments. We are a one-stop solution for all the c-GLP compliant advanced analytical solutions. We specialise in “In-Vitro Bioequivalance - a battery of unique, advanced techniques for same ness establishment in the complex pharmaceutical dosage domain”. We are USFDA inspected and approved multiple times and have a clean track record of compliance. The 90 plus highly qualified analytical scientists at INVITRON provide comprehensive solutions to pharmaceutical and biotechnology firms for the product development process ranging from formulation, CMC support, to batch release and post approval stability for submission to regulatory agencies worldwide. Our speciality services that support the customers include Method Development, Validation and Transfer, Extractable & Leachable analysis, QC Release Testing, In-Vitro Bioequivalence package, Q3 (Micro) Structural characterization, ICP-MS Elemental Analysis, Particle Morphology, Rheology Studies, Impurity profiling and Characterization, IVRT/IVPT Studies, Product De-Formulation Studies, Protein and Peptide Characterization, Stability Testing Studies, In-Vitro Bioequivalence Package, Combination Products Testing and Medical Devices Testing. We are committed to consistently deliver regulatory compliant advanced analytical services of highest quality standards exceeding set expectations. Quality is our job, Analytical testing is our passion, Customer satisfaction is our maxim and Co-operation is our motivation. To know more about INVITRON Advanced Analytics, visit https://invitron.co.in or reach out to us at bd@invitron.co.in!