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The life sciences practice at ClearBridge provides strategic advice and consulting services to the biotechnology, pharmaceutical, medical device, and clinical industries.
Our strategic and operational expertise helps companies overcome challenges in clinical data management, validation, regulatory approval and most aspects of drug development.
Our areas of focus include:


  • Clinical Operations
  • Clinical Research
  • Quality Assurance
  • Regulatory Compliance
  • Verification and Validation
  • Safety / Pharmacovigilence
  • 3rd party manufacturing
  • Purchasing
  • Research & Development
  • Product Development
  • SOP generation
  • PMO support

Additionally, we are well versed in the implementation and validation of life sciences and medical device technologies to include:

  • Clinical software systems (Oracle Clinical), Enterprise Resource Planning (SAP, Oracle, JDE)
  • Laboratory Information Management Systems (StarLIMS, LabWare, Applied BioSystems)
  • Corrective Action Preventative Action (CAPA) systems (TrackWise, EZ-CAPA)
  • Document Management Systems (Documentum, QUMAS, LiveLink)
  • Adverse Events Systems (ARISg, Argus Safety).

We approach all of life sciences projects with the goal of improving your organization as a whole while helping you deliver increased services and financial performance.


To learn more about our Life Sciences practice:

Email: This email address is being protected from spambots. You need JavaScript enabled to view it.
Phone: (781) 916-2284 or toll free (877) 808-2284