Bio Pharmaceutical Development Services

We are offering pharmaceutical development & manufacturing health biotech supports cgmp finish formulation development product manufacturing with sterile fill and finish, with separate process development laboratory, filling, lyophilization and finish to support production of biopharmaceuticals. Health biotech research centre's (hbrc's) scientists use quality-by-design (qbd) tools at early as well as late stages of formulation development. Use of design of experiments (doe) along with risk assessment strategies helps us to design our experimental plan which is scientifically valid and targeted for completion within our delivery timelines. Contract process development services : process development for small molecule, injectables and biologics laboratory scale, pilot scale, cgmp clinical trial materials and cgmp commercial scale process optimization,technology transfers formulation development formulation development for injectable and lyophilized products (clinical to commercial) process development, optimization and upstream downstream processing lab & pilot scale process development test batches manufacturing for stability studies, test and analysis clinical packaging & labeling hbrc has team of expert scientist with rich experience in biotechnology, pharmaceuticals and nanobiotechnology,synchronized for successful development of technology and finish formulations. Hbrc's scientists have extensive multinational expertise developing formulations for conventional and specialized dosage forms, including sustained (sr) & modified release (mr) solids, liquids, and injectables. Pharmaceutical finished formulation are developed keeping in view product stability, compatibility and patient compliance in custamarized way following quality by design (qbd) approach. All of the formulation are designed and developed for techno-economical feasibility and commercialization success.