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Guided by the drug Marketing Authorization Holder (MAH) system and combined with the company's own advantages, we integrate the resource elements of the whole life cycle of drugs, and build a complete closed-loop service system from project initiation, research and development, domestic and foreign registration, raw material procurement, production to sales and service.
In order to ensure the success of the project, the company has set up a leading domestic drug research and development institution and formed an experienced team with more than 10 years of practical experience. Our team is able to develop and undertake a wide range of dosage forms including tablets, capsules, oral solutions, dry suspensions, ointments, eye drops, pre-filled needles, water needles, freeze-dried and more. The independent quality department is responsible for the development and implementation of the company's quality management system and provides strict horizontal supervision of project research and development. With a quality management system covering the whole life cycle of drugs, the company provides comprehensive and effective quality assurance for all stages of drug research and development - from project initiation, pharmaceutical research, clinical research organization management, registration, commissioned production management, pharmacovigilance, marketing, product distribution and inventory management - to ensure that the research and development process follows scientific norms, and Integrity and reliability of experimental data.
Through business communication and collaboration with drug manufacturers, clinical trial institutions, drug operators, medical institutions, etc., we have accumulated rich experience. We are committed to providing consumers with reliable, high-quality medicines that meet the changing market demands and the health needs of consumers.