Quality system

Quality system
As an outstanding manufacturer of chondrointin sulfate in China, we pride ourselves on an unfailing commitment to quality, always with the goals of our customer in mind and knowing that the health of the consumers will be relying on what we manufacture.
Our Quality Assurance and Regulatory team is broadly experienced in the industry and has many years of combined knowledge applicable to a cGMP environment. Strong support is provided for:
● Document development
● Validation
● Quality Systems
● Product disposition
● CMC and other regulatory services

Our staff is well versed in regulatory audit support and pre-approval inspection preparation and is ready to work with our customers to assure the highest probability of success for product registration.

Our manufacture complies with the requirements of ICH Q7 GMP for active pharmaceutical ingredients. We establish, document, and implement an effective system for managing quality that involves the active participation of management and appropriate manufacturing personnel.
The system for managing quality encompasses the organizational structure, procedures, process and resources, as well as activities to ensure confidence that our product will meet its intended specifications for quality and purity.
All quality-related activities are defined and documented.
We establish a quality unit that is independent of production and that fulfills both quality assurance (QA) and quality control (QC) responsibilities.