In-house courses

We offer in-house courses online, on-site or at a location near you. Find your course in our standard course catalogue, or make an inquiry below for a customized course based on your specific training needs.  

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Refresher training
In-house training

Customized In-House training

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Refresher training concepts

Choose from 5 popular concepts designed for in-house refresher training. Theory combined with competitions and practical tasks, where everyone is involved and has fun in the meantime!
READ MORE →

Re-training in GMP – how to make it an effective learning activity!

Watch the free webinar presented by Anna Lundén (25 min)

GMP Re-training

Customer feedback

Envirotainer RelEye RAP

”When we needed a common training in root cause analysis for personnel from both engineers, manufacturing teamleaders, purchasers and auditors we chose GBA Key2Compliance to deliver it for us.

The training was a great success, not least because the flexibility from GBA Key2Compliance to adjust the sessions for our needs, the possibility to add real-world cases to train on between the sessions as well as a truly competent and inspiring trainer/teacher. I can definitely recommend them for your next training event!”

Sofie Nordhamren
Quality Director
Envirotainer Engineering AB

Browse our standard courses​

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Acceptance Sampling Plans: Inspection by Attributes

Get an understanding of the terminology and goals of acceptance sampling plans without delving deep into the statistical theory. Part 2.
Statistics

Acceptance Sampling Plans: Inspection by Variables

Get an understanding of the terminology and goals of acceptance sampling plans without delving deep into the statistical theory.
Statistics

Advanced Training in Biological Evaluation of Medical Devices

Learn how and when a biological evaluation, according to ISO 10993-1, should be performed. Understand the evaluation requirements and avoid common pitfalls!
Biocompatibility

Alfa Laval Live Cleaning-in-Place Experience & Site Tour

Experience Cleaning-in-Place (CIP) technology in action, incl. sustainability-focused cleaning processes, real-life trials, with experts in cleaning validation.
cleaning in place, Sterilization

Applying Control Charts for Visualizing and Detecting Trends

This webinar will provide a valid statistical procedure that is so simple, you won’t even know that you are applying statistics -- all the time.
QC-lab, Statistics, Validation and Qualification

Are Your Data Normal or Not?

What is “Normal” data? How do you know if your data are Normal? What do you do if your data are not Normal? Why would you care?
Statistics

Auditor / Lead Auditor – 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.
- Jun 25, 2026
Auditing/Inspection

Auditor/Lead Auditor – Läkemedel och medicinteknik

Denna specialanpassade utbildning ger dig de verktyg och färdigheter som krävs som Auditor eller Lead auditor inom läkemedels- och medicinteknisk industri.
- Mar 5, 2026
Auditing/Inspection, Validation and Qualification

Avvikelseutredning och CAPA i läkemedelsindustrin

Lär dig om CAPA och alla steg som en avvikelse passerar: initiering, utredning, design av åtgärder, effektuppföljning och rapportskrivande. Undvik fällorna!
CAPA

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.
GLP

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.
- Feb 5, 2026
Biocompatibility

Becoming a Regulatory Affairs Manager for Medical Devices

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.
- May 7, 2026
Post market, Quality management and QA, Regulatory Affairs

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

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

CE-marking – Risk classification of IVDs & Technical Documentation

Learn about the new rule-based risk classification. Understand how the risk classification impacts on the conformity assessment route Learn about the general safety and performance requirements and how to demonstrate compliance Understand the structure and content of the Technical Documentation Understand how design changes to the product design impact on the technical documentation
CE-marking, Documentation, IVD, IVDR, Risk

CGMP för kvalitetskontroll (QC) och analysarbete

Fördjupningskurs med specialinriktning mot krav på kemisk och mikrobiologisk kvalitetskontroll under utveckling (klinisk fas) och tillverkning av läkemedel.
QC-lab

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