Menu

Life Sciences - Medical Devices & Pharma

Home / Life Sciences - Medical Devices & Pharma

The capability to keep it simple yet effective

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
David P
October 8, 2025
The Medical Device Regulation (CE Marking Process Key Updates)
I think virtual (online) works well and it is useful for hearing the perspectives of other course participants
Jenny A
October 7, 2025
ISO 13485:2016
Very good informative day Anne Marie was a brilliant trainer
James P
October 7, 2025
ISO 13485:2016
Anne Marie was very knowledgable on the 13485subject and provided extra information on other standards
Lisa M
October 7, 2025
ISO 13485:2016
Great course. Questions were answered when asked. Learned a lot.
Damien H
October 7, 2025
ISO 13485:2016
Great course very well delivered with lots of great interaction.
Paul D
October 7, 2025
ISO 13485:2016
Well worthwhile
Cecilly T
October 7, 2025
ISO 13485:2016
It was really good overall! The breakdown of each section made the information much easier to understand. It also clarified which sections apply to specific tasks in my role, such as supplier management.
Read more reviews

Public ProgrammePublic Programmes

In-Company ProgrammesIn-Company Programmes

Life Sciences - Medical Devices & Pharma

NEW

Quality Systems and Regulations

Validation

Software Validation

Risk Management

Testing and Calibration

Technical Writing

Internal Auditing

Cleanroom

GMP

Hospital & Medical