GMP Certification
Passed GMP Compliance Inspection for Pharmaceuticals
National Medical Products Administration
QUALIFICATIONS
Awards & Honors
GMP-certified with drug registration certificates and patented inventions. Backed by a MAH platform and CNAS-accredited testing, our quality management system covers the entire process from raw material procurement to finished product release.
4
Number of Qualification Categories
8
Total Certificates
QUALITY
Quality Management System
Every step from raw materials to final release is fully traceable with complete documentation.
Jiangsu Tianping Pharmaceutical has established a comprehensive quality management system and strictly adheres to GMP standards for production and quality control. From raw material sourcing and in-process controls to finished product testing, the company implements end-to-end traceability to ensure every batch meets regulatory requirements and customer specifications.
Our company employs a professional quality inspection team and advanced testing equipment, offering full-scope testing capabilities for raw materials, auxiliary materials, packaging, intermediate products, and finished goods to ensure product quality.
GMP Certification
Medical Device Production License
Jiangsu Provincial Medical Products Administration
GMP Certification
MAH Holder System Certification
National Medical Products Administration
Drug Registration
Drug Registration Approval (23 MAH-listed drugs)
National Medical Products Administration
Quality Certification
CNAS National Laboratory Accreditation
CNAS (China National Accreditation Service for Conformity Assessment)
Quality Certification
ISO 13485 Medical Device Quality Management System
International Organization for Standardization
Corporate Honors
High-Tech Enterprise Certificate
Ministry of Science and Technology
Corporate Honors
Jiangsu Province Specialized and New "Little Giant"
Jiangsu Provincial Department of Industry and Information Technology
DOCUMENTS
For detailed qualifications
Contact us for GMP certificates, registration approvals, test reports, and other qualification documents required for collaboration.