We’ll guide you through the standards and regulations required for compliance, their practical implementation and auditing, as well as the risk management associated.
What Our Learners Say
Tiffany M
February 18, 2026
ISO 13485:2016
Really enjoyed the course. Kevina is passionate and very knowledgeable and delivered the course in a efficient manner
Dagnija Z
February 10, 2026
Good Laboratory Practice (QMS ISO 17025:2017)
Informative, vast subject to be covered
Muazam I
February 10, 2026
Good Laboratory Practice (QMS ISO 17025:2017)
It’s very good to get iso knowledge related to quality management
Rula A
February 10, 2026
ISO 15189 Internal Quality Auditing of Medical Laboratory Quality Management Systems
Very good
Jowita C
February 5, 2026
Mastering CAPA in the Medical Device Industry
The CAPA course was extremely helpful and well‑structured. The content was clear, easy to follow, and directly connected to real work situations. John explained each step of the CAPA process in a simple and practical way, which made it much easier to understand and apply. I feel more confident in identifying issues, analysing root causes, and choosing the right corrective or preventive actions. Overall, the training was 100% satisfactory.
Catherine M
February 5, 2026
Mastering CAPA in the Medical Device Industry
Had a really great time and feel as though I was able to take in all of the information and that I can confidently apply it in my working life.
Jennifer O
February 3, 2026
IH Custom Course Life Sciences
AnneMarie was amazing. So patient, knew the answer to everything we asked and explained it in a way we could clearly understand. 5 stars 🌟
Lynn T
February 3, 2026
IH Custom Course Life Sciences
Ann-Marie is so knowledgable and gave us so much valuable information on MDR compliance. I would highly recommend her for all of your medical devices training needs.
Public Programmes
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