The Regulatory Department is responsible for cooperating the applicant for the registration of human drugs, veterinary drugs, pesticides and chemicals to submit an application to the relevant supervision and administration department in accordance with legal procedures and relevant requirements, and the supervision and administration department reviews the safety, effectiveness and quality of the intended marketing of human drugs, veterinary drugs, pesticides and chemicals, then makes a decision on administrative licensing.

The Regulatory Department has always been committed to providing customers with professional registration documents to ensure that customers get marketing authorization for human, veterinary, pesticide and chemical products, so as to support the smooth business negotiations.

With rich registration experience, we can provide regulatory registration and consultation in the local market, such as USFDA, Anvisa, EDQM, MAPA, REACH etc. Especially the registration of APIs, pesticides & feeds and chemicals in the Brazilian and European markets. We have assisted customers in completing more than 120 drug registrations, 19 MAPA registrations, and 175 EU REACH registrations. Further we can track and maintain lifecycle management of the entire project registration process.