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  • Go back
  • Drug Substance Development (API)
  • Drug Product Development​
  • Manufacturing Operations
  • Manufacturing Compliance
  • Go back
  • Development Strategy​
  • Program Evaluation
  • Non-Clinical Study Execution
  • Non-Clinical Regulatory Submissions
  • Non-Clinical Compliance
  • Go back
  • Clinical Development Strategy
  • Clinical Operations & Study Management​
  • Medical Writing & Regulatory Submissions
  • Clinical Compliance​
  • Go back
  • Pre-Approval
  • Authoring, Publishing & Submissions
  • Post-Approval
  • Functional Outsourcing
  • Special Projects
  • Go back
  • Strategy Development
  • Achieving Market Access
  • Go back
  • Artwork & Labeling​
  • Distribution
  • Product Release Process
  • Pre-Approval Inspections & Vendor Audits
  • Go back
  • Good Laboratory Practice (GLP)
  • Good Clinical Practice (GCP)
  • Good Manufacturing Practice (GMP)
  • Inspection Readiness
  • Go back
  • Organizational Assessment, Strategy & Design
  • Implementation, Excellence & Transformation
  • M&A Regulatory Due Diligence & Integration
  • Digital Technology Advisory
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    Contract Opportunities

    NEW: GxP Vendor Audit Services

    Contract: 48 weeks

    Reference: 5723

    Apply Now

    Exclusive to The Source - register/apply now

    Immediate request:

    Please provide pricing for any audits you have experience in.

    The Role

    • Outsourced GCP audits, GLP audits and non-critical GMP audits.
    • Requirement may also include GCLP, GVP and CSA, with combinations and potential GCP mixed into some audits.
    • GDP may be required in the future.

    Requirements

    How to Apply

    This contract opportunity is exclusive to The Source.

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