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Clinical trial materials manufacturing services and specialized technologies to support clients in early pharmaceutical development through phase IIIa clinical trials; sterile injectables, ophthalmics, otics, tablets, capsules, solutions, suspensions, semi-solid, and other dosage forms.


Our investment in state-of-the-art facilities and highly trained experts emphasizes our commitment to delivering positive customer experiences across all phases of pharmaceutical and biopharmaceutical development. From early-stage research and development, to clinical trial materials production and GMP manufacturing support, we are dedicated to providing the best, and most reliable analytical testing services. Pace Analytical® Life Sciences is well-equipped to handle almost any project regardless of scope or complexity.

Literature, Accreditations & Documentation

  • FDA Registered
  • DEA Registered (Class II-V)
  • GMP Compliant
  • ISO 17025 Accredited

Where and how we Work

Pace Analytical Life Sciences operates five state-of-the-art facilities providing  CMC Pharmaceutical development and manufacturing (CDMO) services FDA-registered, cGMP-compliant contract research organization (CRO) services. Each of our facilities have long-established histories of very successful product development and commercialization with excellent audit outcomes from both regulatory agency and partner-client reviews.

  • CRO Laboratory

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