ISO 14001:2015 Requirements E-Learning

A brief four-hour, flexible interactive electronic learning package on ISO 14001:2015.

• Other sectors

ISO 22301:2019 Requirements E-Learning

An e-Learning course of four hours in total covering the basics of business continuity management systems.

• Other sectors

ISO 9001 Implementor E-Learning

A half-day online course covering the basics of ISO 9001 and Quality Management Systems.

• Other sectors

ISO Main Features E-Learning

A very brief e-Learning course on the fundamentals of ISO High-Level Structure.

• Other sectors

ISO/IEC 27001: 2022 Awareness E-Learning

A self-paced eLearning course on ISO/IEC 27001:2022 explaining the overview of the standard requirements

• Other sectors

MDR training E-Learning

A one-day e-Learning course covering the differences between Medical Device Regulation EU 2017/745 compared to the Medical Device Directive.

• Other sectors

Requirements Course on ISO 9001:2015 for Quality Management System

An e-Learning course of four hours in total covering the requirements of ISO 9001:2015 Quality Management System.

• Other sectors

Risk Based Approach E-Learning

A two-hour course leading to a better understanding on the concept of risk management.

• Other sectors

What are SDGs and How to adopt them in your strategy? E-Learning

A very brief online course providing basic knowledge on the relationship between ISO standards and Sustainable Development Goals.

Environmental Management System Auditor/Lead Auditor kursus i forhold til ISO 14001:2015 | CQI IRCA-certificeret Kursus-ID: 17913

Dette 5-dages kursus giver den viden og de færdigheder, der er nødvendige for at organisere og lede audits af miljøledelsessystemer. Vores erfarne undervisere guider dig igennem hele auditprocessen fra udarbejdelse af auditprogram til afrapportering af auditresultater. Undervisningen tilrettelægges som en kombination af teoretiske indlæg, rollespil, gruppearbejde og diskussion. Kurset afsluttes med en kompetencegivende eksamen.

• Food and beverage

FSMA Preventive Controls Qualified Individual (PCQI)

This course is developed by the FSPCA and has the “standardized curriculum” recognized by FDA. Successful completion of this course is the way to meet the requirements for a “preventive controls qualified individual.” (PCQI)

• Food and beverage

FSSC 22000 Version 6 Lead Auditor Training Course based on ISO 22000:2018 (English)

Formålet med dette kursus er at give deltagerne den nødvendige viden og de nødvendige færdigheder til at udføre første-, anden- og trepartsaudit af fødevaresikkerhedsledelsessystemer i henhold til ISO 22000:2018 og FSSC 22000 version 6, i overensstemmelse med ISO 19011, ISO 22003 og ISO 17021, hvor dette er relevant. CQI- og IRCA-certificeret kursus Ref: 2409

• Food and beverage

FSSC 22000 Version 6 Transition Course

Transition course design to understand the key changes of the FSSC 22000 version 6 as compared to FSSC 22000 version 5.1 of the scheme.

• Food and beverage
• Other sectors

Hazard Analysis and Risk Assessment (HARA) Training

Discover the HARA training by DNV and gain essential knowledge of hazard analysis and risk assessment principles. Click here.

• Food and beverage
• Other sectors

IFS Food Standard Version 8 Training

Kurset dækker de overordnede krav i version 8 af IFS Food.

• Cyber security
• Other sectors

Information Security Management System Auditor/Lead Auditor Training Course as per ISO 27001 | CQI and IRCA Certified Course ID: 17325

Formålet med dette kursus er at give de nødvendige færdigheder og viden til at udføre første-, anden- og trepartsaudit af informationssikkerhedsstyringssystemer i henhold til ISO/IEC 27001 (med ISO/IEC 27002) i overensstemmelse med ISO 19011 og ISO 17021, hvor det er relevant.

• Other sectors

Introduction to biocompatibility for medical devices

This training will provide participants with an insight into biocompatibility, risk-based approach ISO 14971:2019, on the ISO 10993-1 and ISO 10993-18 standards.

• Other sectors

Introduction to Business Continuity Management Systems as per ISO 22301:2019

This course is designed to help you and your organisation/institute to understand the requirements of the Business Continuity Management System and specific requirements as stated in the ISO 22301:2019 standard.

• Other sectors

Introduction to IVDR EU 2017/746 In Vitro Medical Device Regulation Training

The In Vitro Medical Device Regulation (2017/746) entered into Force in 2017 and has date of application May 26, 2022. This course provides a knowledge of the requirements of the regulations including the requirements for Technical Documentation and Quality system requirements.

• Other sectors

Introduction to MDR EU 2017/745 Medical Device Regulation

The revised Medical Device Regulation (2017/745) entered into Force in 2017 and has date of application May 26, 2021. This course provides a knowledge of the requirements of the regulations including the requirements for Technical Documentation and Quality system requirements.

• Other sectors

IRCA Certified ISO 13485:2016 QMS Lead Auditor Training for Medical Devices

This intensive ISO 13485 lead auditor course is a key requirement for becoming a registered Lead Auditor. Achieve an internationally accepted CQI/IRCA (Charted Quality Institute - International Register of Certificated Auditors) registered certificate.

• Other sectors

ISO 13485:2016 and Medical Device Regulation (MDR) Internal Auditor Course

You will learn the principles and practices of effective quality management process audits in accordance with ISO 13485:2016, the MDR and ISO 19011:2018. You will be taken through the entire audit process from planning the audit to reporting and follow up on non-conformities.

• Other sectors

ISO 13485:2016 Foundation Course

This course clarifies ISO 13485:2016 requirements and interpretations. Organizations that need to show evidence that they can provide medical devices which consistently meet customer and regulatory requirements will benefit from understanding ISO 13485.

• Other sectors

ISO 13485:2016 Internal Auditor Course

This internal auditor training course you will learn the principles and practices of effective quality management process audits in accordance with ISO 13485:2016 and ISO 19011:2018.

• Cyber security
• Other sectors

ISO 27001:2022 Internal Auditor Training Course

This course aims to provide you with the opportunity to learn about the subject of internal auditing of information security management systems, specifically those based on the ISO 27001:2013 international standard.

• Other sectors
• Corporate
• Automotive and aerospace

ISO 30415:2021 ISO 30415 Diversity and Inclusion Course For Managers

Et otte timers kursus i to sessioner, der giver et grundlæggende overblik over mangfoldighed og inklusion som beskrevet i ISO 30415:2021.

• Other sectors

ISO 31000 Risk management – foundation course

A one-day course focusing on understanding the key elements of ISO 31000 as the basis for good risk management practice.

• Other sectors

ISO 45003 - Psychological Health and Safety at work Training course

On this one-day training course, you’ll learn how to manage psychosocial risks across your organization as part of your overall occupational health and safety management system based on ISO 45001.

• Other sectors

ISO 55001:2024 Awareness Course

The overall aim of the ISO 55000 series is to assist an organisation in optimising and improving the management of business assets.

• Other sectors

ISO 9001 foundation course

The purpose of the course is to provide participants with a basic knowledge of quality management systems and the requirements of the ISO 9001 standard.

• Other sectors

ISO 9001:2015 Internal Auditor Training

The aim of the course is to provide you with knowledge of the entire audit process and plenty of practice in delivering effective internal audits that create value for the organization.

• Cyber security
• Other sectors
• Healthcare
• +7

ISO/IEC 42001 Artificial Intelligence Management System (AIMS) Internal Auditor course

Discover ISO 42001 Internal auditor training course by DNV and learn how to plan and conduct an AIMS audit according to ISO/IEC 42001 requirements.

• Other sectors

ISO/IEC 42001: 2023 Artificial Intelligence Management System Foundation

This course provides participants with knowledge of the ISO/IEC 42001 Artificial Intelligence Management System requirements and its benefits

• Finance
• Other sectors
• Cyber security
• +6

ISO/IEC 42001:2023 Requirements Course

This course is designed as an introduction to the basic purpose and structure of the ISO/IEC 42001:2023 Information technology - Artificial intelligence Management system standard.

MDR-audit – intern auditor i relation til MDR

Få viden om de MDR-krav, der ikke er omfattet af ISO 13485, og forstå MDR-kravene i relation til QMS og deres indvirkning. Lær, hvad du skal være opmærksom på, når du auditerer et QMS i forhold til MDR-kravene.

• Other sectors

MDSAP - Medical Device Single Audit Program

This course pack is designed to give you a detailed understanding of the medical device single audit program.

• Other sectors

OHSMS Auditor/Lead Auditor course based on ISO 45001 | CQI IRCA Certified Course ID: 1877

This course is designed to develop a clear understanding of safety management in the modern era and provide those involved in audit conduct and management with the skills to fulfil their role.

• Other sectors

Person Responsible for Regulatory Compliance (PRRC)

You will learn what you need to know about the role as PRRC, which is mandatory for Medical and In Vitro Diagnostic Device Manufacturers. We will get knowledge of what the role covers and how this role should be implemented from a regulatory perspective.

• Other sectors

Post Market Surveillance

This course will give an introduction to the regulations and guidance on PMS (plan and report) as well as the process interfaces.

• Other sectors

QMS Auditor/Lead Auditor Training Course (ENGLISH)

This course is designed to provide participants with the knowledge and skills required to perform first, second and third party audits of management systems against the requirements of the ISO 9001:2015.

Quality Culture

Et effektivt ledelsessystem er kernen i en effektiv virksomhed og driver virksomheden frem mod sine strategiske mål. Det effektive ledelsessystem bør derfor forholde sig til sine interessenters behov og forventninger, risici og muligheder, lovkrav og ikke mindst organisationens værdier og kultur.

• Other sectors

Risk Management ISO 14971:2019

This course will give an overview of the standard, the process and the tools. The process interface and the resource needs will be part of the course along side a workshop on risk analysis.

Sikker udvikling af sundhedssoftware gennem overholdelse af IEC 81001-5-1

Udvikl sikker sundhedssoftware, der opfylder EU's og FDA's forventninger. Dette kursus viser dig, hvordan du anvender IEC 81001-5-1 i praksis, styrker din trusselsmodellering og risikostyring og skaber en cybersikkerhedsramme, der kan skaleres på tværs af din organisation.