Our endeavor is to achieve distinction by sustaining the premier excellence values in all its manufacturing units. The entire production process is conceded out under austere observation and quality measures. The company operates following preset equivalence of USFDA, UKMHRA and PIC's Quality Management System standards and is in the process of attaining all these.

Our fundamental aim is to manufacture and deliver quality tested products; for which we have well established Quality Assurance and Quality Control departments for practical & proactive quality checks that further helps us to deliver medicines of international quality and foster steadfast association with esteemed patrons.

In-house quality control laboratories, chemical, instruments, microbiology & pharmacology laboratories that are fully equipped with state of the art instruments (manufactured by well-known multinationals) like High Performance Liquid Chromatography System (WATERS), Gas Chromatography System (HP), Ultraviolet Spectrophotometers (SHIMADZU), Infra-red Spectrophotometers (PE) & Other Laboratory instruments.

Raw material, packing material, in-process, finished products & stability analysis are carried out for ensuring the quality at each & every step of manufacturing. Each product is being tested for safety, quality & efficacy.

Quality assurance department, a fully autonomous functionality is in place to keep track of each activity, parameters & processes to achieve the quality goal in totality. Quality of each medicinal product is assured by applying TQM techniques by the QA-Team. QA Team is having professionals with Doctorates & 10-20 years experiences from multinationals in the same functionary.

Our focus is monitoring of good manufacturing practices at each and every stage of manufacturing and quality control departments, selection and control of Raw Material and Packing Material.

REGULATORY AFFAIRS

Making all systems adhering to international regulatory requirements & generation of technical data in line with regulatory requirements & submission of dossiers to various countries are being managed by well qualified, experienced & trained professionals at international level team. Team is capable to conduct all sorts of experiments & generation of such data for submission to international authorities for medicinal product approval.