Regulatory support

Regulatory support
We have a professional regulatory team which gives adequate support to our product and customers all the time. According to the requirements of market authorization in different countries or regions, we prepare corresponding application files and establish the regulatory systems.
At present, we are taking part in the NPA-GMP certification Program，the Natural Products Association is the USA’s largest and oldest non-profit organization dedicated to the natural products industry
For the regulatory affairs in European countries, COS certification and EDMF will be conducted.
In order to support the pharmaceutical registration in FDA of USA, DMF and site inspection will be prepared.
For the supporting quality files (COS/EDMF/DMF), they are prepared according to the requirements of different countries or regions and in ICH CTD format (i.e. ICH M4Q), so as to ensure the good progress of the product registrations of our end users.