Gulf Biotech 3.52

Gulf Biotech offers a broad range of parenteral fill and finish "Contract manufacturing" services and can support your compound throughout the entire sterile manufacturing process.

We Offer Formulation and product Development support to optimize pre-formulated API, as well as to identify the strongest of several prequalified drug formulations. In addition to formulation support, we have capability for Process design and development. A comprehensive range of services designed to meet your goal of a fast, smooth transfer of your project in the clinical phase through to commercial manufacturing.

A broad range of production services are offered for clinical trial material, from compounding to primary packaging to filling / lyophilizing, Scale-up from the small-scale process developed in the lab to a commercially viable and robust process using a Quality by Design approach. Expertise in lyophilisation scale-up, commercial scale process, formal GMP validation, stability batches, and regulatory support at each step are also developed in house.