1. Quality Policy
Insist on implementing the new version of GMP, insisting on "excellent products to customers, health to you and me, and green to the society".
1. Establish a quality management system, clarify the responsibilities of each department, divide the responsibilities, and decompose and implement;
2. Provide necessary resources to create conditions to ensure the establishment of a quality system;
3. Actively organize employees to receive training to improve their professional quality and quality awareness;
4. Strive to make every batch of products meet the company's quality requirements;
5. Strictly implement GMP, standardize management, strengthen assessment, and ensure the effective and normal operation of the quality system;
2. Quality objectives
Produce qualified products and comprehensively improve the level of production management and quality management.
3. Quality Assurance
1. Strictly implement the national "Drug Production Quality Management Regulations" (2010 Edition), "Drug Administration Law", "Drug Administration Law Implementation Regulations" and "Drug Registration Management Law" and related quality regulations to ensure product quality.
2. Responsible for establishing a complete quality assurance system to ensure the effective operation of the quality assurance system.
3. Responsible for the quality control of the entire process of product procurement, acceptance, production, warehousing, sales and after-sales, timely feedback, investigation, and handling opinions and reports on problems arising in the process.
4. Responsible for the investigation, implementation and reporting of quality accidents, product complaints and product returns.
5. Review quality standards, product process regulations, batch records, inspection procedures and quality assurance-related documents.
