Through collecting abroad resources (team and technology), taking advantages of local land (hardware, people, and capital), Redpharm (Beijing) biopharmaceutical Institute Co., Ltd is devoted to injecting new power into the R&D field of global biological pharmaceutics, accelerating the transfer of fundamental research to clinical drugs, and becoming a significant pivot that interlinks the R&D of global biological drugs and the downstream clinical development.
Promote effective R&D system. Accelerate the transfer of blood type biological products to clinical drugs.
Insist on ‘combining the generic and the innovative’ R&D guidance. Exert a long-term influence from the origin on the R&D of global new drugs.
Redpharm aims at building up a huge global production network. The R&D and production base in Qingdao is a very important component of this ‘global production network’. The R&D and production bases in Qingdao and North America form the foundation of R&D and production system.
The R&D production base of Redpharm (Qingdao) locates in Qingdao ‘Sino-German Ecopark’ where the international top companies converge. This base aims at R&D and production of high-end biological products. Phase I project covers an area of 100 mu, the investment of which is up to 160 million dollars. It will be designed and constructed as an integrated base of production, training, and research for biological products, represented by oxygen carrier Haemoglobin.
Redpharm always insist on the purpose of maximizing the benefit of clients and patients, collaborating closely with internal and external scientific research institutes, providing the optimal solutions of local production for clients and patients, and making efforts to realize synergistic effect increase.
Redpharm establishes and perfects the integrative management and control system. We control our production through a digital system, realizing programmed control of production, automation of testing, channelization of transportation, and mechanization of packing.
Organize production in strict compliance with GMP rules. Strengthen the quality supervision and management throughout the production process. Establish quality supervision and testing agencies with first-class equipment for quality testing to form complete and accurate quality supervision and management system.