Genovior is capably of developing protein process for the products, either new or generic biologics, initiated by clients for clinical application or for filing purposes for commercial productions in a timely fashion and under economical budgeting. Genovior can also efficiently and effectively tech-transfer microbial process, both up-stream and down-stream to our facilities from customers.
Genovior provides high quality services for finished products of vials in liquid or lyophilized forms, prefilled syringe, cartridge, and dual chamber syringe/cartridge. PIC/S or US FDA guidelines are strictly followed in our facilities. We can also provide services for development of lyophilization program as well as design of packaging box, labeling of randomized code and labels, and packing of the final product.