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A Guide to Validation Managers and Calibration Managers in Pharmaceutical Companies

A Guide to Validation Managers and Calibration Managers in Pharmaceutical Companies

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The role of the Validation & Calibration Expert is to ensure that facilities, instruments, and processes are qualified, calibrated, and validated in accordance with international standards.
This operational guide walks you through ISO 17025 and the DQ/IQ/OQ/PQ qualification requirements, providing practical tools to face audits and maintain compliance.

What you’ll find inside:

🔬 ISO 17025 explained clearly and applicable to day-to-day operations
📊 DQ/IQ/OQ/PQ qualifications presented step-by-step with real examples
Checklists for process and method validation
🚀 Common audit findings and how to effectively defend your position

Each section is enriched with diagrams, operational tables, and real case studies to minimize the risk of non-compliance.
A complete manual designed for professionals in Technical QA, Validation, and Maintenance, who need clear, concrete references to manage complex activities.

Format: Professional PDF
Length: 186 operational pages
Updated: 2025 – includes references to the latest ISO and EU GMP revisions

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Available languages: ITA – ENG

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DECLARED REGULATORY BASIS

Built on the most up-to-date official sources.

Every guide is built from the official sources current at the editorial verification date stated in the document. The editions, revisions and cut-off dates used are declared and checked again for every new release; requirements are kept distinct from GuideGxP operational interpretation.

Main references for this guide EU GMP Annex 15 · ICH Q9(R1) · GAMP 5 (2nd ed.)
  • Editions and revisions stated in the document
  • Explicit editorial verification date
  • Requirements separated from practical recommendations

GuideGxP is an independent publisher and is not affiliated with, approved by or sponsored by the authorities and organisations cited.

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Buy once: whenever we publish a new release of the guide you purchased, it is sent automatically to the email address used for the order, together with the download link. No request, new registration or additional payment is required.

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  • Average review cycle: 6 months

Timing may vary with regulatory and technical developments. No action is required after purchase; simply use a valid email address at checkout.

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