Norescience Consulting is specialized in regulatory affairs compliance at NMPA providing services for medical devices, drugs, IVD, food, cosmetics registration.
Gathering professionals with extensive expertise, Norescience has accumulated years of experience providing services for medical devices, drugs, cosmetics, IVD registrations, clinical trials, devices testing,and additionally, performing studies for device marketing entry.
The company has rich experience in clinical trials, CER and registration of high-end medical devices. We can provide various services for different customers with the development of our company. We count with standard Animal Labs and clinical experimental centers where are well equipped providing services for Chinese hospitals, which give us more confidence to provide great services for your company in China.
Norescience gathers different kinds of professionals, relying on support of colleges, universities, scientific research institutes, testing institutions, clinical institutions, certification institutions and relevant experts or scholars, integrating the advantages of all parties, inheriting the spirits of professional, rigorous, honest enterprise, and striving to become the leader of medical equipment industry, also, creating new value for the medical industries.
Quality and tranparency are the principle of our services. When working with us, you will use reliable resources to benefit your business.
Having a business with Norescience means that you will own a full range of professional services and successes!
Latest news and information
Circular of the center for drug examination of the State Food and Drug Administration on Issuing the technical requirements for pharmaceutical researc
(Trial) (No. 21, 2021)Date of issue: 20210308In order to further guide enterpris...
2021-03-10 vcc 14
Notice of the State Food and Drug Administration on the implementation of the provisions on the administration of cosmetic registration and filing mat
In order to implement the relevant provisions of the regulations on the supervis...
2021-03-10 vcc 12
Announcement of the State Food and Drug Administration on adjusting part of the contents of the classification catalogue of medical devices (No. 147, 2020)
In order to further deepen the reform of the review and approval system of medic...
2021-02-02 vcc 10
Circular of the State Food and Drug Administration on Issuing 7 guiding principles for registration technology review, including the guiding principles for registration technology review of household
In order to strengthen the supervision and guidance of the registration of medic...
2021-02-02 vcc 14