We provide cGMP clinical supplies manufacturing, packaging, and labeling services for domestic and international distribution studies. Entrust your liquids, suspensions, and semi-solids to our experts so your clinical trials can continue with ease.
Pace® is open to supporting unique dosage form and manufacturing processes.
Our manufacturing facilities meets FDA, cGMP, and EU requirements for Phase I and II clinical supplies, and are licensed with the Drug Enforcement Agency to manufacture and test controlled substances. We designed our facilities to handle a variety of manufacturing challenges such as potent compounds, light sensitive compounds, and organic solvent processing.
On-Demand Webinar: Suspension Formulation
Connect with Pace® to learn how we can customize manufacturing process trains to meet specific product needs.
Solutions, Suspensions, & Semi-Solids
Solutions & Suspensions
- Oral, topical, pediatric, and fixed dose combinations
- Creams, gels, and ointments
Packaging & Labeling
- Bottles, blisters, tubes, jars, and sachets
- Open labels, blinded labels, and simple kitting