Projects Intro

CE&IC has successfully completed hundreds of GMP development and manufacturing projects for our bio/pharmaceutical clients. Our primary practice areas include Biologics, API’s, Sterile Fill/Finish, Oral Solid Dosage forms, Liquid Dosage forms, and Highly Potent Compounds. Within these practice areas, we can assist our clients in delivering their projects from planning and concept development through preliminary and detailed design, procurement, construction assistance, commissioning and validation.

Please find following an overview of CE&IC’s capabilities within each of these practice areas.

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