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!
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.
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?
Nov 18
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.
Oct 21
- Oct 23, 2025
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.
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.
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.
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.
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.
Online
CAPA, Quality management and QA

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.
Nov 5
- Nov 7, 2025
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

Contamination control in cleanrooms for Life Science production

Learn the necessary EU and US requirements (regulatory and technical) to control contamination in production or research operations in cleanrooms.
Cleanrooms and cleaning, Sterile products

Contamination Control Strategy

The necessary requirements to control contamination in sterile production or research.
Cleanrooms and cleaning, Sterile products

Cybersecurity in Medical Device Lifecycle

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

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