I will review your gmp sop, batch record for audit readiness

Regulatory inspections dont forgive weak documentation and your GMP SOPs and batch records are the first thing auditors examine.

If youre preparing for FDA, EMA, MHRA, WHO, or internal audits, your documentation must be clear, compliant, and inspection-ready.

I will professionally review your GMP SOP or batch manufacturing record to identify compliance gaps, formatting issues, inconsistencies, missing elements, and audit risks before an inspector does.

• Is your SOP aligned with current GMP requirements?
• Does your batch record demonstrate traceability and data integrity?
• Are you confident it will withstand a regulatory inspection?

You're in the right place.

What I Review:

• GMP compliance alignment (FDA / EU / WHO standards)
• Data integrity & ALCOA+ principles
• Clarity, structure, and logical flow
• Deviations, corrections & documentation practices
• Risk areas that trigger audit findings
• Formatting and consistency
• Missing critical compliance elements
• Version control & change management check

Why Choose Me?

• Strong understanding of GMP documentation standards
• Audit-readiness focused approach
• Clear, structured written feedback
• Confidential and professional handling of documents

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