CFDA-医疗器械注册证
The official registration certificate required for medical devices sold in China.
ISO 14001: 2015
International standard for establishing effective environmental management systems.
ISO/IEC 27001:2022
A global standard for managing and protecting information security within organizations.
ISO 13485:2016 – Medical Device QMS
It ensures compliance with international standards for quality management in medical devices.
MDR Implementation Training Course
It certifies expertise in implementing and complying with EU MDR requirements.