Public courses

GBA Key2Compliance solves all your training needs in terms of regulatory requirements, GMP, GXP and quality systems for pharmaceutical & medical device industry.

Below you can browse our upcoming trainings, both on-site in Northern Europe and online. Our network of experts cover a wide range of important and contemporary topics to meet your needs. 

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Risk Management for Medical Devices – ISO 14971 – Course

Get a good insight and understanding of the key requirements for a risk management system in compliance with EU regulations.
Sep 22
Online
Risk

Sterilization of Medical Devices Course

In-depth training on assessing suitability, adequacy and effectiveness of medical device sterilization methods.
Oct 1
- Oct 7, 2026
Copenhagen, Denmark
Auditing/Inspection, Bioburden, ISO 11737, Sterilization, Validation

Becoming a Regulatory Affairs Manager for Medical Devices – Course

Get the knowledge and skills needed to lead the RA function at a medical device organization. Interpret and apply MDR, IVDR, and ISO 13485 effectively.
Oct 6
- Oct 7, 2026
Copenhagen, Denmark
Post market, Quality management and QA, Regulatory Affairs

GMP MasterClass course

Get a comprehensive review of GMP compliance requirements and tools to master application and interpretation of these requirements in pharmaceutical production.
Oct 7
- Oct 8, 2026
Copenhagen, Denmark
GMP, Pharmaceuticals, QC-lab, Quality management and QA

Basic course in GLP – Good Laboratory Practice

Get the basic knowledge and understanding needed for working in a GLP environment. Learn to find your way in the OECD GLP and other relevant guidances.
Oct 8
Online
GLP

Cybersecurity in Medical Device Lifecycle – Course

How to have your Medical Devices compliant with the cybersecurity requirements: risk management, design, development, maintenance, and post-market surveillance.
Oct 12
Online
Computers/Software

Change Management for Medical Devices – Course

How to apply a risk-based approach when managing changes to your medical device to ensure compliance, maintain quality, and ultimately protect patient safety.
Oct 13
Online
Change management, Risk

Usability for Medical Devices – Course

How do you know if the users think your device is “Easy to use”? Learn how to establish, implement and monitor a usability process.
Oct 14
Online
Usability

Test Method Validation (TMV) Made Easy – Part 1 Variable Measurements

How do you know you have quality if you cannot reliably measure what you are doing? Are you afraid of complex statistical concepts and procedures? These two webinars will help you to evaluate your measurement systems, diagnose problems, and fix them. How is it “made easy”?
Oct 20
Online
Statistics, Validation and Qualification

Design and development of Medical Devices

A course to understand how to design and develop medical devices to ensure their safe and effective use.
Oct 21
- Oct 22, 2026
Copenhagen, Denmark
Design Control, Medical devices

Test Method Validation (TMV) Made Easy – Part 2 Attribute Measurements

This second webinar will focus on Attribute Measurement Systems – that is, the subjective inspection of items to see if they satisfy requirements. Since humans are the “gauges”, attribute measurement systems can have high variation. How do you evaluate this human judgement and how can you improve their results? And how is it “made easy”?
Oct 21
Online
Statistics, Validation and Qualification

Process validation – Medical Devices – Course

Gain increased knowledge about both the preparations required and the main parts that are included in process validation for medical devices.
Oct 22
Online
Validation, Validation and Qualification

Cleaning validation of pharmaceutical process equipment – Course

Learn details for all part of the global cleaning validation strategy in pharmaceutical activities. CGMP expectations, technical and regulatory updates.
Nov 3
- Nov 5, 2026
Copenhagen & Kolding, Denmark
Cleanrooms and cleaning, Sterile products, Validation and Qualification

Strategic communication course

Get tools for clear communication about e.g. requirements and expectations in different situations. Be seen as a positive leader that inspires quality work.
Nov 4
- Nov 5, 2026
Copenhagen, Denmark
General, Quality management and QA

Auditor / Lead Auditor Course – Pharmaceuticals and Medical Devices

This tailor made training gives you the tools and skills required as Auditor or Lead Auditor in the Pharmaceutical and Medical Device industry.
Nov 9
- Nov 11, 2026
Copenhagen, Denmark
Auditing/Inspection

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