Our sterile manufacturing facility in Charleston, South Carolina, is home to scientific and technical staffs with years of experience in the development and manufacture of parenteral products. The U.S.- and E.U.-compliant and DEA-licensed manufacturing facility can deliver batches for clinical studies and niche commercial markets. Finished product forms include liquids, lyophilized products, suspensions, emulsions and terminally sterilized vials.  Our team has experience with both small and large molecules (proteins, peptides, monoclonal antibodies and other large molecules). One of the benefits of our operational setup is the seamless integration of our manufacturing facilities with our on-site packaging and distribution facility.  For clinical trial supplies, we provide custom packaging, labeling and kitting – including distribution and QP services for materials destined for trials anywhere in the world.

We provide expert support for randomization and blinding studies, including placebo, comparator and crossover studies. We also provide reconciliation drug accountability and destruction service as needed.

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Contact us for more information about our Parenteral services.