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Pace Analytical Life Sciences (PLS) provides raw material testing services to the pharmaceutical, biopharmaceutical and medical device industries. We offer excipient testing to support USP/NF, EP, BP, JP, FCC and ACS monograph testing requirements. We also can test following client-supplied or vendor supplied methodology. Our raw material testing supports formulation development within research and development, excipients and active pharmaceutical ingredients used in finished product manufacturing and supports the qualification of our client’s raw material vendors.

Our Raw Material Testing services include:

  • Complete Compendia Testing (USP, EP, BP, JP, FCC, ACS testing)
  • USP <467> Residual Solvent Testing
  • HPLC, GC and IC analyses
  • Spectrophotometric Analyses (FTIR, UV/VIS)
  • Metals Analyses (AA, GFAA, ICP)
  • Heavy Metals Testing
  • Ethylene Oxide and 1,4 – Dioxane Testing
  • Container Testing per USP <661> and <671>
  • Purified Water and Sterile Water for Injections Testing
  • Karl Fisher Analyses
  • Wet Chemistry Analyses

We also provide active pharmaceutical ingredient testing.

We understand that our clients need results of their raw materials accurately and quickly. To that end we offer expedited turn around time services so that our clients can count on getting their results to meet their “just-in-time” manufacturing processes.

Pace Analytical Life Sciences brings years of experience performing all types of analytical testing on raw materials and active pharmaceutical ingredients. We maintain the highest level of quality and attention to detail to our clients to assure that their raw material testing will be successfully executed and that their results will be delivered on time. We also offer rush turn- around time service for those times when results are needed quickly.

We are FDA registered, DEA registered, cGMP compliant, and ISO/IEC 17025 accredited.

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Pharmaceutical Testing

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