Pace Analytical Life Sciences’ GMP testing lab has been collaborating with clients to develop pharmaceutical, biopharmaceutical, and medical device products for over 20 years.

Pace Life Sciences provides full-service, extensive drug analysis capabilities with concomitant process understanding, by leveraging analytical methods, physicochemical, biophysical, and/or biopharmaceutical characterization. The combination of our team’s experience and our cutting edge, GMP, FDA approved facilities allows us to assist our clients to analyze their novel drug entities. Our customers also have access our secure laboratory data management system. Click here to learn more.

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Pace provides our customers with a full-service, extensive small molecule analysis capabilities, by leveraging advanced analytical methods. The combination of Pace’s experience and cutting edge, GM

Pace Analytical Life Sciences offers testing services to support the biopharmaceutical manufacturing industry. Our team of experts and our extensive selection of testing equipment offers you the services and expertise to

Pace Analytical Life Sciences is a full-service contract analytical testing laboratory providing microbiology testing services to the pharmaceutical and medical device industries. PLS has expertise in testing many

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 (United States

Pace Analytical Life Sciences offers full-service laboratory capabilities for assessing levels of elemental impurities in raw materials, in-process formulations, finished products, and medical devices. Elemental met

Pace Analytical Life Sciences (PLS) operates a state of the art contract analytical laboratory that provides stability testing and stability storage support to the pharmaceutical, biopharmaceutical and medical device

Pace Analytical Life Sciences (PLS) has developed a comprehensive approach toward extractable and leachable testing. PLS designs studies to identify extractables, compounds that can be extracted from a

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WEBINAR: Extractables and Leachables of Biopharmaceutical Container Closure Systems

As biopharmaceutical drug product development continues to grow, so do new regulations on packaging and container closure components associated with delivery of the drug product to the patient. This webcast will present a brief introduction to extractables and leachables (E&L), followed by a discussion of relevant United States Pharmacopeia and ISO guidelines and practical considerations when planning an extractables and leachables project.

Topics covered in this webinar:

  • Review results and analysis of an E&L case study of biopharmaceutical single-use bag systems
  • Gain an overview of the process, procedures, and approaches for biopharma E&L studies
  • Understand analytical capabilities and expertise needed to conduct effective studies

Speakers:

Daniel Abate, Ph.D.
Principal Chemist.
Pace Labs
Hannah Tims, PhD.
Principal Chemist.
Pace Labs