Shenzhen Feifei Medical Device Registration Consulting Co., Ltd. is a specialized focus on the domestic registration of medical devices (including standard preparation, product testing, clinical trials, system / specification assessment, registration and approval) of the emerging consulting company, but also to provide production licenses, business licenses, the new, replacement, change, product technology development, transfer and cooperation, clean plant design and construction. ISO13485, GMP, CE, FDA and other certification consulting. Our consultants and expert team have experience in senior management positions in large and medium-sized medical device manufacturers and professional background in product registration and certification auditing. They are well versed in the operation mode and industry characteristics of medical device manufacturers, and are proficient in relevant laws and regulations, as well as management standards and technical specifications, and have a strong advantage in the areas of regulatory guidance, standard understanding, product testing, document preparation, product improvement and professional translation. We have strong advantages in regulatory guidance, standard understanding, product testing, document writing, product improvement, professional translation, etc. We have friendly cooperative relationships with well-known international certification bodies in the UK, US, Germany, Switzerland and other countries, as well as domestic authoritative certification bodies and testing organizations. Our services have been widely recognized by our customers.
Our aim is to create value for our customers.
We are characterized by: professional and fast.