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Environment, Health and Safety Management Systems Training

Comply Guru offer Environmental, Health and Safety (EHS) Management System Training that is available in multiple formats from eLearning, Blended Learning or Instructor-led Learning to help you or your organization.

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2025 Training Guide

Innovation Leaders for ISO Standards, Auditing & Medtech QA/RA Training

2025 Training Guide

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ISO 14001 + ISO 45001 Lead Auditor Training

Environment, Health & Safety

ISO 14001 + ISO 45001 Lead Auditor Training

48-62hrs CQI-IRCA Cretified Course
ISO 14001 Internal Auditor Training

Environment, Health & Safety

ISO 14001 Internal Auditor Training

16-24hrs CQI-IRCA Cretified Course
ISO 45001 Internal Auditor Training

Environment, Health & Safety

ISO 45001 Internal Auditor Training

16-24hrs CQI-IRCA Cretified Course
ISO 14001 Foundation

Environment, Health & Safety

ISO 14001 Foundation

7hrs CQI-IRCA Cretified Course
ISO 45001 Foundation

Environment, Health & Safety

ISO 45001 Foundation

7hrs CQI-IRCA Cretified Course
ISO 14001 Essentials

Environment, Health & Safety

ISO 14001 Essentials

2hrs
ISO 45001 Essentials

Environment, Health & Safety

ISO 45001 Essentials

2hrs
ISO 14001 Lead Auditor Training

Environment, Health & Safety

ISO 14001 Lead Auditor Training

40-48hrs CQI-IRCA Cretified Course
ISO 45001 Lead Auditor Training

Environment, Health & Safety

ISO 45001 Lead Auditor Training

40-48hrs CQI-IRCA Cretified Course
ISO 14001 + ISO 45001 Internal Auditor Training

Environment, Health & Safety

ISO 14001 + ISO 45001 Internal Auditor Training

24-40hrs CQI-IRCA Cretified Course

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.

Why does CAPA get a bad rap in the Medical Device Industry?
Why does CAPA get a bad rap in the Medical Device Industry?
Michelle Keane discusses CAPA in Medical Devices including potential reasons organizations struggle and the FDA raise so many findings in this area....
As per ISO 13485, is Spreadsheet Validation required?
As per ISO 13485, is Spreadsheet Validation required?
As per ISO 13485, is it true or false that a medical device organization that uses spreadsheets is only required to validate spreadsheets that contain...
Comply Guru Sponsors Global Access 2024
Comply Guru Sponsors Global Access 2024
Comply Guru proudly sponsored Global Access 2024 which is 's largest conference for Quality and Regulatory Affairs Professionals in Medical Devices....

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CQI & IRCA Approved Training Provider

CQI & IRCA Approved Training Provider

Offering certified courses since 2019

Exemplar Global Recognized Training Provider

Exemplar Global Recognized Training Provider

Offering certified courses since 2020