Quality Management System (QMS) Training

Comply Guru offer Internationally Accredited Quality Management (QMS) Training with the Chartered Quality Institute (CQI), International Registrar of Certificated Auditors (IRCA) offering credentials for any Industry that are globally recognized.

Comply Guru offer different types of training courses depending on the target audience and training needs. We can also tailor training to meet your company’s specific needs or requirements. Our courses are available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization.

CQI-IRCA Certified Course Exemplar Global Certified Course RAPS Certified Course
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ISO 9001 Internal Auditor Training for Quality Management Systems (QMS)
4.6 ★★★★★ 203 Reviews
ISO 9001 ISO 19011 Quality Management

ISO 9001 Internal Auditor Training

16hrs
CQI-IRCA Certified Course
Price: €595.00

ISO 9001 Internal Auditor Training is for anyone that wants to be part of the team that conducts internal audits of part of their Quality Management System based on ISO 9001:2026.

ISO 9001 Lead Auditor Training for Quality Management Systems (QMS)
4.7 ★★★★★ 137 Reviews
ISO 9001 ISO 19011 ISO 17021 Quality Management

ISO 9001 Lead Auditor Training

40hrs
CQI-IRCA Certified Course
Price: €1195.00

ISO 9001 Lead Auditor Training is for anyone that wants to gain the knowledge and skills required to perform full system first, second and third-party audits of quality management systems against ISO 9001:2026, in accordance with ISO 19011:2026 and ISO IEC 17021-1:2015.

ISO 9001 Requirements for Practitioners and Auditors
4.6 ★★★★★ 223 Reviews
ISO 9001 Quality Management

ISO 9001 Requirements Training

7hrs
CQI-IRCA Certified Course
Price: €395.00

ISO 9001 Requirements Training is for anyone looking to gain a comprehensive understanding of the core requirements of ISO 9001 and this highly interactive course can be completed anytime, anywhere (24/7).

ISO 17025 Internal Auditor Training for Laboratory Quality Management Systems
4.9 ★★★★★ 8 Reviews
ISO 17025 Quality Management Laboratory

ISO 17025 Internal Auditor Training

16hrs
Exemplar Global Certified Course

ISO 17025 Internal Auditor Training is for anyone that wants to be part of the team conducting internal audits of part of their ISO 17025 (2017) Accreditation.

ISO 17025 Requirements Training for Laboratory Quality Management Systems
ISO 17025 Quality Management Laboratory

ISO 17025 Requirements Training

7hrs
Exemplar Global Certified Course

ISO 17025 Requirements Training is for anyone that wants to gain a good understanding of the ISO IEC 17025 (2017) Requirements.

ISO 19011:2026 Transition Training
ISO 13485 ISO 9001 ISO 45001 ISO 14001 ISO 19011 Medical Devices Quality Management Environment, Health & Safety

ISO 19011:2026 Transition

120mins

ISO 19011:2026 Transition Training provides a detailed overview of the changes introduced in ISO 19011 and their practical implications.

Introduction to ISO 9001 Training
4.6 ★★★★★ 261 Reviews
ISO 9001 Quality Management

Introduction to ISO 9001

45mins

Introduction to ISO 9001 Training is for organizations looking for a concise, high-level introduction for their staff.

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WHAT'S NEW

2026 Training Guide

Transformational Training for ISO Standards, Auditing & Medtech QA/RA

2026 Training Guide

Read, Watch & Discover More

Our team has you covered with expert insights & updates to stay on top of the latest updates, trends, and changes in the industry.

Design Controls, Design and Development under FDA QMSR
Design Controls, Design and Development under FDA QMSR
Michelle discusses Design Controls, ISO 13485 Design and Development and what endures under the FDA's QMSR in effect from February 2026....
Reaffirmed, Not Static: ISO 13485 and the Global Regulatory Evolution
Reaffirmed, Not Static: ISO 13485 and the Global Regulatory Evolution
Michelle discusses the recent affirmation of ISO 13485:2016 and shares her insights on the new guidance reflecting a Global Regulatory Evolution....
Low Risk Does Not Mean No Risk
Low Risk Does Not Mean No Risk
Michelle discusses why ISO 13485 and ISO 14971 make a critical clarification on Risk, and clarifies a dangerous misconception in medical device develo...

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