Pace Analytical Life Sciences Clinical Trial MaterialsWith Pace, you have a partner who understands the unique requirements of your business and industry; one who can provide the technical expertise, innovation and world-class facilities that enable you to bring products to market faster and meet all the current quality, health and safety standards. For more than 30 years, Pace has been advancing candidates from early pre-formulation and tox studies to an IND filing and on through the clinical phases. Our extensive GMP clinical supplies manufacturing capabilities include oral/solid/liquid and topicals capabilities, sterile fill-finish and clinical packaging and kitting for a variety of molecules/dosage forms.

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On-Demand Webinar: Formulation Strategies for Early Clinical Phase Studies Watch our Webinar Watch our Webinar Pace Analy ...
Our aseptic manufacturing facility meets FDA (Food and Drug Administration) cGMP (current Good Manufacturing Practices) and EU (European Union) requirements for Phase 1 and 2 clinical trial product manufacture. The aseptic fill facility is monitored, controlled and recorded in real-time and servi ...
We provide cGMP clinical supplies manufacturing, packaging, and labeling services for domestic and international distribution. Dosage Forms Oral Solid Dosage Tablets Immediate release, sustained release, delayed release, chewabl ...
We provide cGMP clinical supplies manufacturing, packaging, and labeling services for domestic and international distribution. Liquids & Semi-Solids: Solutions Oral, topical, pediatric, and fixed dose combinations Suspensions ...
At Pace we offer small scale feasibility and cGMP pilot scale spray drying for drug bioavailability enhancement. Production of amorphous solid dispersions via spray drying is a commercially proven approach to boosting bioavailability for poorly soluble drugs. Pace can rapidly assess the feasibili ...
A strong suite of analytical services is essential to effective delivery of high-quality clinical supplies. Every step of process development, formulation development, and the manufacturing of clinical trial materials requires a series of good decisions based on good analytical data to keep your ...