What we can do: the registration service for APIs, excipients, the innovative drugs, generic drugs, imported drugs, international multi-center clinical trial applications, CRO consultation, supplementary application/additional information, re-registration, as well as regulatory consulting, technical guidance and etc. Our Team, working in this field for over 20 years, is an experienced team with professional expertise and familiar with the technical requirements and regulatory requirements of the registration.
Pharma-orange is a trusted partner for taking all activities relating to your registration of drugs in China. Phamra-orange always stands by customers to achieve the goals with three criteria:
Pharma-orange has been cooperated and supported many customers from India, European countries to proceed the registration procedures in accordance with the regulations of CFDA. The products that our team got the IDL successfully are as follows but not limited to: Glibenclamide, Clomiphene, Fosinopril, Paroxetine, Perindopril and etc.