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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CAPA and root cause analysis, tools for an effective CAPA process – Course

Review the key requirements for Corrective Action and Preventive Action (CAPA), explore common industry practices.
May 18
Online
CAPA, Quality management and QA

Design of Experiments – DOE – Course

What parameters are key to quality? How do we quickly and efficiently identify these parameters and decide on strategies to optimize quality?
May 25
Online
Design Control, Statistics, Validation and Qualification

GMP Basics for ATMP – Course

This training is an introduction to GMP requirements for both manufacturing of investigational ATMP and ATMP with a marketing authorisation.
May 26
Online
ATMP, General, GMP

GMP Master Class (Svensk version) – Kurs

Lär dig att förstå, navigera, tolka och tillämpa GMP enligt krav i både EU och USA, samt ICHs guidelines för kvalitetssystem och kvalitetsriskhantering.
May 28
- May 29, 2026
Stockholm, Sweden
Quality management and QA

Introduction to GMP and Quality Systems – Course

Gain essential Good Manufacturing Practice (GMP) and Quality Management System (QMS) skills to succeed in regulated Life Science industries.
Jun 2
Online
General, GMP

Strategisk kommunikation – Utveckla din roll som QA – Kurs

Vi går igenom verktyg för att på ett tydligt sätt kunna kommunicera ut till exempel krav och förväntningar i olika situationer. Dessa verktyg hjälper QA-personal att ses som positiva ledare som inspirerar i kvalitetsarbetet.
Jun 9
- Jun 10, 2026
Stockholm, Sweden
Quality management and QA

Validering och kvalificering – Kurs

Få fördjupade kunskaper om de regulatoriska kraven kring validering och kvalificering vid läkemedelstillverkning och hur de appliceras.
Jun 10
- Jun 11, 2026
Stockholm, Sweden
Validation and Qualification

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.
Jun 11
Online
GLP

Auditor / Lead Auditor – Pharmaceuticals and Medical Devices – Course

This tailor made training gives you the tools and skills required as Auditor or Lead Auditor in the Pharmaceutical and Medical Device industry.
Jun 23
- Jun 25, 2026
Copenhagen, Denmark
Auditing/Inspection

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.
Jun 24
Online
Usability

Software Assurance and validation of software for QMS process – Course

Learn the concepts of QMS software validation, how to assess risks related to QMS software and how to apply IQ, OQ and PQ to QMS software.
Sep 3
Online
Computers/Software, Validation and Qualification

Basic Training in Biological evaluation of Medical Devices

Get fundamental knowledge to understand how and when a biological evaluation, according to ISO 10993-1, should be performed and avoid the most common pitfalls.
Sep 8
Online
Biocompatibility

Statistical Techniques for Process Validation Made Easy – Part 1

Learn how valid statistical techniques contribute to Process Validation efforts. Best practices for quality systems in industry.
Sep 9
Online
Statistics, Validation and Qualification

Statistical Techniques for Process Validation Made Easy – Part 2

Learn how valid statistical techniques contribute to Process Validation efforts. Best practices for quality systems in industry.
Sep 10
Online
Statistics, Validation and Qualification

MDSAP – a global audit approach – Course

Learn how to plan perform and report internal MDSAP audits as well as best practice and tools how to be prepared to undergo or perform MDSAP audits.
Sep 15
- Sep 16, 2026
Copenhagen, Denmark
Auditing/Inspection, Medical Device, Quality management and QA

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