The QC testing of drug compounds is performed on a worldwide scale by pharmaceutical companies, contract research labs (CRO) and various other institutions. Regulatory requirements are broader and more stringent than ever before and will only increase to protect human and nature. With the Current Good Manufacturing Practices (cGMPs) for human pharmaceuticals quality standards are set to insure product quality and safety. Adherence to the cGMP regulations assures the identity, strength, quality, and purity of drug products by requiring that manufacturers of medications adequately control manufacturing operations. Reproducible, reliable and robust methods of analysis play a vital role in regulatory compliance.
Antec Scientific ALEXYS Analyzers are used worldwide to meet USP and EP regulatory and safety standards for a broad range of compounds. Dedicated Analyzers have been developed offering exceptional sensitivity, selectivity, and throughput for aminoglycoside and macrolide antibiotics, (di-) sulfides, glycoproteins, carbohydrates and many other pharmaceuticals.