Pace is able to offer a wide range of testing services. Our team and facilities can handle nearly any environmental analysis you need, regardless of scope complexity or logistics.
Almost any kind of biological sample can be analyzed.
Our list of certifications and accreditations provides you with nationwide coverage to meet environmental compliance requirements or to support engineering.
Pre-formulation characterization and formulation development services for complex pharmaceuticals and biologic therapies. GMP clinical trial materials manufacturing with specialty spray dry dispersion and lyophilization process development services.
Formulation development, process development and specialty services (spray drying, nano milling, hot-melt extrusion and lyophilization) to manufacture phase I/phase II clinical trial materials (CTM).
Provides the highest-quality chemistry and microbiology testing services following current good manufacturing practices (cGMP) to support complex pharmaceuticals, biologic, and drug-device combination therapies.
Flexible scientific staffing solutions allowing you to focus on your core business and respond to workload demand.
The regulatory services team provides expertise in the areas of hazard communication, product stewardship and raw material data management to companies of all sizes both domestic and globally.
With over 20 years of experience our instrument support services help optimize your efficiency and control costs.
Biocompare, The Buyer’s Guide for Life Sciences Published an Article: The Changing Landscape of Gene Therapy, written by Frank Tagliaferri, Ph.D., VP of Pharmaceutical Development & GM at Pace® Life Sciences (PLS).
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