OUR SERVICES
Regulatory training/Talent Cultivation
● Medical Device Quality Management System Internal Auditor Training (ISO 13485 (GB/T 42061), China GMP, US 21 CFR Part 820 (QSR/QMSR), EU MDR, MDSAP)
● Medical Device Management Representative Training
● Medical Device Risk Management Training (ISO 14971 (GB/T 42062))
● Biological Evaluation of Medical Devices Training (ISO 10993 (GB/T 16886))
● Medical Electrical Equipment - General Requirements for Basic Safty and Essential Performance (IEC 60601-1 (GB 9706.1)) Training
● Medical Device Usability Engineering Training
● Medical Device Clinical and Animal Trial Full-Process Compliance Training
● Medical Device Design Development and Quality Assurance Training
● Medical Device Professional Technical Knowledge Training (Sterilization Processes/Cleanroom Environment/Process Water Systems, etc.)
● Medical Device Specialized Testing Technology Inspector Training
● Customized In-house Training for Medical Device Enterprises
TELEPHONE
（+86）-755-26910212
cjh@szmdqa.org
ADDRESS
Room 3E,3/F,JiuZhou DianQi Building,KejiNan 12 Road,KejiYuan,NanShan District,
Shenzhen,Guangdong,P.R.China 518063
2014-2026 Shenzhen Medical Device Quality Promotion Association. All rights reserved
