Overview
1 Carry out the laws and regulations on drug quality management, and organize and standardize the quality control of pharmaceutical production.
2 Establish the company\'s quality assurance system and quality control system and monitor its operation.
3 Authorize the quality management documents.
4 Authorize the process validation and key process parameters.
5 Authorize the internal control quality standards for materials and finished products.
6 Set standards for nonconforming product handling.
7 Authorize the product recall.
8 Organize the investigation of quality accident and quality issue, and report to the drug supervision and Administration Bureau.
9 Supervise the implementation of quality responsibility system and reward and punishment system at all levels of quality department; pay close attention to quality education, and carry out the assessment of quality consciousness of department heads.
All the best! - 
