

iBio Consulting
Technical SOP Writing and Review
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SOP Gap Assessment
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Write new SOPs tailored to the client’s actual lab workflows, instrumentation, and regulatory environment.
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Edit legacy SOPs for clarity, technical accuracy, and updated compliance standards.
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Redline documents to show changes and rationale for QA or regulatory reviewers.
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Align SOP content with current lab practices and roles (avoid “document says one thing, staff does another” situations).
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Facilitate interviews with scientists, QA personnel, and lab managers to capture real workflows.
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Lead or participate in review meetings to gather feedback and reach consensus on procedures.
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Bridge communication gaps between QA and technical staff to ensure SOPs are both rigorous and usable.
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Audit SOPs for traceability, consistency, and inspection readiness.​