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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.  

Standard Courses

Choose from 5 popular concepts designed for in-house refresher training – with competitions and practical tasks everyone is involved and have fun in the meantime!

Refresher training
Inhouse training

Customized In-House training

To tailor the course to your needs, we would like you to take these questions into account when contacting us. 


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  • How many participants do you want to take part in the training?

  • Are there any specific routines that need improvement?

  • Would you like a verification test after the training?

  • Extent of the training, and preferable timeframe?

  • Online or as a on-site course at your location?

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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

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

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.
- Oct 23, 2025
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.
- Jun 26, 2025
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.
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.
- Apr 30, 2025
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

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

Change Management for Medical Devices

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

Cleaning validation of pharmaceutical process equipment

Learn details for all part of the global cleaning validation strategy in pharmaceutical activities. CGMP expectations, technical and regulatory updates.
- Nov 7, 2025
Cleanrooms and cleaning, Sterile products, Validation and Qualification

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