Focus on researching regulations of domestic and international pharmaceutical and health product
Integrated practical experience and knowledge of pharmaceutical administration and regulation
Professional employees are all graduated from well-known pharmaceutical universities, dedicated in R&D and registration of drug for a long time
Built close partnerships with the professional consultants for domestic and international medical regulations
Provision of registered agent (import registration)
Evaluation for feasibility of imported drugs, medical instruments and special medicine products etc.,
Reviewing, revising and guide the registration materials
Organizing and submitting application information of CTD format
Assist on registration inspection, quality standard reviewing and sample delivering
Assist on registration inspection, quality standard reviewing and sample delivering
Assist on purchasing standard and reference products
Track and follow whole progress during registration
Answer the questions of registration declaration and regulations