From Innovation to Market Faster with Pace Analytical Life Sciences

Leading the Industry in Quality Testing for Regulated Industries

Pace Analytical Life Sciences offers cGMP-compliant analytical support from discovery through critical development phases to market release for pharmaceutical, medical device and combination drug-device products.

Pace Analytical Life Sciences’ four major divisions – Microbiology, Chemistry, Physical Testing, and Stability Storage and Testing – offer product analysis via client-specific methodologies, USP testing, ASTM, BP and other compendial methods. Please visit the Scope of Services page for a full listing of available tests.

From Innovation to Market Faster with Pace Analytical Life Sciences

Pace Analytical Life Sciences leads the industry in quality testing for regulated industries, but retains the flexibility to customize services to meet each customer’s needs.

Focused on Quality Assurance

Pace Analytical Life Sciences has a robust quality assurance program, Quality Assurance personnel provide oversight to all areas of expertise. The QA department is comprised of highly trained professionals who are involved in the implementation of quality standards that include a Quality Assurance review and approval of reports. In addition, QA performs internal audits, process audits and critical phase audits. The QA department will work, in consultation with you, to ensure your testing meets and exceeds regulatory requirements (cGMP, GLP, GCP, etc.).

Anticipating FDA Compliance Guidelines

Pace Analytical Life Sciences anticipates market change and regulatory developments by investing in people, innovative technology and processes. For example, when the FDA released compliance guidelines for aseptic processing, Pace Analytical Life Sciences invested in Microbial characterization systems for genotype bacterial identification.