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GLP Clinical & Nonclinical Quality (PK & Tox)

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Before deciding to use a Contract Research Organization (CRO), sub-contractor, or vendor we conduct an on-site inspection of the GLP compliance status and provide you a report of the strengths and weaknesses of the organization from a regulatory compliance standpoint.

Includes

  • CRO Audit
  • Protocol Reviews
  • Data and Report Audits
  • In-Process Study Inspections
  • Facility Inspections
  • Standard Operating Procedures
  • GLP Implementation
  • GLP Training
  • Regulatory Inspection Preparation
pharmaceutical risk assessment