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Our Services

Team Advantage

Redpharm has international teams localized in United States, Canada, and Hong Kong, they are familiar with the United States and the European Union, Canada drug administration laws and regulations; professional staffs are from domestic well-known pharmaceutical companies, and front-line technical and management personnel have rich experience in production, quality management.

Professional advantage

Redpharm Regulatory Affair section focuses on compliance of regulatory, registration of drug and relevant healthcare product; based on registration of our own products, meanwhile, we provide drug administration compliance, pharmaceutical and related health products registration consultation services for both domestic and foreign medical peers.

Information superiority

We Redpharm trace in time and grasp the forefront information and the latest policy updated by state authorities on drugs, medical devices and veterinary medicines. A powerful database of information and document templates has been established.

Channel superiority

Redpharm maintains close contact with the FDA and EDQM in Europe to keep track of the latest regulatory changes. We established a stable relationship with international medical regulations, not only for understanding the impact of regulatory changes on actual application and master international market demand information.

Involving Field

Redpharm can supply services including CEP(TSE)certificate consulting, international drugs registration, and contract R&D and manufacture services that are omnibearing and integrated for protide(including proteins, polypeptide and mAbs).