Liquid Dose Manufacturing

Implementing Medium And High-Volume Drug Handling And Packaging Programs

Simplify the complexity of combination product development by partnering for integrated support across device design, industrialization, manufacturing, and final product assembly.

Don't Just Launch Your Molecule, Protect It!

Accelerate your path to market with integrated support to streamline processes, reduce delays, and deliver safe, user-friendly drug-delivery solutions.

Signant Health, formerly CRF Bracket

The best technology succeeds in the background. Signant Health provides solutions that simplify every step of the patient journey to make it easier for people to participate in, and for sites and study teams to run, clinical trials.

Integrity Bio

Provide help to those who strive to save or improve the quality of human life by providing them the integrated services of Formulation Development, GMP Fill Finish Services, and Innovative Drug Delivery technologies.

Haupt Pharma AG

With nine sites in Germany, Italy, France and Japan, and a representative office in the U.S., Haupt Pharma is one of the largest European companies for pharmaceutical contract development and manufacturing.

Kemwell Biopharma

With manufacturing locations in Bangalore India, and Uppsala Sweden, Kemwell offers the entire value chain from early & late stage drug development services, clinical trial supply support, to commercial contract drug manufacturing.

Laureate Pharma

Laureate Biopharma is a leader in biopharmaceutical contract development and manufacturing. Our scientists are expert in process development and cGMP production of therapeutic proteins, including monoclonal antibodies and Fc-fusion proteins.

Pharmaceutical Contract Manufacturing And Packaging: Creams, Lotions And Gels

Aphena Health & Beauty has the ability to blend a wide range of viscosities from aqueous based to crèmes, lotions, liquids, gels and powders. 

ADME SGS’ Life Science Services provides an extensive pharmacokinetic (PK) and pharmacodynamic (PD) support in pre-clinical and Phase I-III clinical studies in accordance with international regulatory standards (FDA, EMEA, ICH).