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Internal Audit Schedule Template

Streamline Your Internal Audit Planning

Rook Quality Systems’ free, customizable Internal Audit Schedule Template is designed to help medical device companies establish and maintain a structured internal audit schedule for their Quality Management System (QMS). This tool ensures that the requirements of the US Quality System Regulation (QSR) 21 CFR 820, ISO 13485:2016, and the EU Medical Device Regulation (EU MDR) are met throughout the internal audit planning process.

Key Features:

  • Customizable – Provided in an editable Word format, allowing you to tailor sections to your organization’s specific regulatory requirements and internal documentation (e.g., SOPs, version numbers).
  • Flexible Audit Approach – Use the template to schedule either full QMS internal or internal process audits, depending on your company’s needs.
  • Regulatory Alignment – Covers key quality system requirements, including FDA 21 CFR Part 820, ISO 13485:2016, and EU MDR 2017/745 to support compliance.
  • Ready to Use – Pre-filled with essential audit elements, making it easy to implement immediately upon download.

Take control of your internal audit schedule and ensure regulatory compliance with ease. Download the template today!

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