Our Core Services:

• Analytical Testing: We offer a range of analytical tests to assess the quality and purity of pharmaceutical substances. This includes identification, quantification, and characterization of active ingredients and excipients using advanced techniques such as chromatography, spectroscopy, and mass spectrometry.
• Stability Studies: We conduct stability testing to evaluate how pharmaceutical products maintain their quality over time under various storage conditions. Our studies ensure that medications remain effective and safe throughout their shelf life.
• Formulation Analysis: Our team examines the formulation of pharmaceutical products to ensure that they meet the required specifications and perform consistently. This includes evaluating physical properties, dissolution rates, and compatibility of ingredients.
• Regulatory Compliance: We provide analytical support to ensure that pharmaceutical products comply with regulatory standards and guidelines. Our expertise helps in preparing and reviewing documentation for regulatory submissions, including quality control data and validation reports.
• Method Development and Validation: We develop and validate analytical methods to ensure accuracy, reliability, and reproducibility in testing. Our methods are designed to meet industry standards and regulatory requirements.
• Contaminant and Impurity Analysis: We identify and quantify potential contaminants and impurities in pharmaceutical products. This is crucial for ensuring product safety and efficacy.
• Quality Assurance: Our analytical services are integral to quality assurance programs, helping to maintain high standards throughout the drug development and manufacturing processes.