In-House Training

Are you a group in need of the same training? Do you wish to customize a standard course to better suit your needs?

All of our public courses are available in-house. We provide customized and tailored courses and training within all our expertise areas. Our team of experts have the knowledge and experience needed to build training sessions relating both to the compliance need of your organisation and type of operation.

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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.
Online
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.
Online
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!
May 19
Mölndal-Gothenburg, Sweden
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.
Kolding, Denmark
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.
Apr 22
Online
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?
Online
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 23
- Jun 25, 2026
Copenhagen, Denmark
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.
May 5
- May 7, 2026
Stockholm, Sweden
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.
Jun 11
Online
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.
Online
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 6
- May 7, 2026
Copenhagen, Denmark
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.
May 12
Online
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
Online
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.
Online
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.
Online
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.
Copenhagen & Kolding, Denmark
Cleanrooms and cleaning, Sterile products, Validation and Qualification

Clinical Evaluation for Medical Devices

Get a good insight and practical guidance on the key steps of performing and how to fulfill the requirements of a Clinical Evaluation.
Online
Clinical development

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