POET is not designed to serve as the system of record for regulated processes, therefore not subject to GxP requirements. It is designed to enable cross‑organizational collaboration and process orchestration while the system of record remains within enterprise systems.

Type = Technical Guides,; Topic = Opus Solution Environment, Process Orchestration for Empowered Teams (POET), Opus Platform,;Persona = Solution Designer, Solution Partner, Technology Partner,; Orchestration = Logistics,; Function = Regulatory Affairs, Quality,

Audits and Inspections

Audits and Inspections enable pharmaceutical organizations to coordinate regulatory inspections and supplier audits across the supply chain network. The solution supports inspection planning, collaboration with external partners, documentation management, and tracking of findings and closure outcomes.

What are Audits and Inspections

Audits and Inspections are structured evaluations conducted internally or by regulatory authorities to assess compliance with quality standards, internal procedures, and applicable regulatory requirements. The audit and inspection process in the pharmaceutical industry typically involves the following steps:

  1. Initiate Inspection Record: Create and log a new inspection record to formally track the regulatory or internal inspection and related activities.
  2. Prepare for Inspection: Gather required documentation, align stakeholders, and ensure systems, processes, and records are ready for the upcoming inspection.
  3. Execute Inspection: Support the inspection by providing requested information, facilitating discussions with inspectors, and documenting inspection activities.
  4. Receive Inspection Report: Record and review the official inspection report detailing findings, observations, or compliance status.
  5. Respond to Observations: Develop and submit responses, corrective actions, or remediation plans to address observations identified during the inspection.
  6. Close Inspection: Complete all required follow-up actions and formally close the inspection once responses are accepted and obligations are fulfilled.

Types of Audits and Inspections

  • Regulatory Inspection: Inspections conducted by health authorities such as FDA, EMA, or other regulatory bodies to verify regulatory compliance.

  • Internal Audit: Audits performed internally to evaluate adherence to company procedures, quality systems, and regulatory requirements.

  • Supplier Audit: Audits conducted to verify supplier compliance with contractual and regulatory obligations.

  • Pre‑Approval Inspection: Inspections conducted prior to product approval or facility authorization.

  • Follow‑Up Inspection: Inspections performed to verify that previous findings or CAPA actions have been successfully implemented.

How to configure the audits and inspections marketplace solution

Before using the audits and inspections solution, configure the solution in OPUS Solution Environment.

Add an audit or inspection

Modify audits and inspections

Monitor audits and inspections

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