VP API is one of the four fonctional management parts of Venturepharm Group. Mainly focus on the providing of contract service, technical support of new products, rare APIs production, consultant to the regular market the companies around the world. The company has mordern API and formulation production bases in Asia for the fully service of its clients.
Wante Venturepharm is the center of AP API. All its production sites comply with the requirements of cGMP, some of its APIs have been sold to the world market by the means of DMF/COS, and got the good reputation of its clients.
VP API strictly follow the GMP requirements of SFDA. It have the whole perfect system of drug registration and quality management, so as to meet those demands of regulatory and clients. All its APIs have passed the SFDA GMP audit of new version.
VP API will fully support of all your work of your expects, such as quality control, technical developing, service, cost reducion, and professional support, commercial confidentail, etc. It knows that the quality is the life of the company, and client is the god, all its work is to fulfil the entirely demands of clients.
VP API declears that, all its products will not violate the patent problems domestic, but will need your responsibility to confirm its patent in the world market. The company only provide research sample and technical support for those within patent products.