PortonBio establishes, implements and maintains a quality system that complies with domestic and foreign GMP regulations. Delivery of products with the quality attributes appropriate to meet the needs of patients, health care professionals, regulatory authorities (including compliance with approved regulatory filings) and customers.
Quality Principle
Quality first, continuous improvement
Quality Objective
100% Regulatory Compliance
100% Product Qualification Rate
Documentation System Architecture Diagram
Quality System Architecture
Quality Commitment
Portonbio's leadership has the ultimate responsibility to ensure that it has an effective pharmaceutical quality system. The quality head of Portonbio leads quality department (QA department) crews to review and approve all quality and GMP related documentation, plans, procedures and records, and monitor the implementation and execution of all GMP activities.