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Quality Systems and Regulations
Home
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Life Sciences - Medical Devices & Pharma
/ Quality Systems and Regulations
Public Programmes
In-Company Programmes
Regulatory Requirements for Importers and Distributors of Medical Devices, EU MDR 2017/745
ISO 13485:2016
Mastering CAPA in the Medical Device Industry
The Medical Device Regulation (CE Marking Process Key Updates)
Understanding QMSR: Key Updates & Compliance Changes
Regulatory Requirements for Importers and Distributors of Medical Devices, EU MDR 2017/745
ISO 13485:2016 & The Medical Devices Regulation (CE Marking Process)
Introduction to Life Sciences Manufacturing
ISO 13485:2016
Mastering CAPA in the Pharmaceutical Industry
Mastering CAPA in the Medical Device Industry
MDSAP: The Medical Device Single Audit Programme
The Medical Device Regulation (CE Marking Process Key Updates)
Navigating Combination Product Regulations
Understanding QMSR: Key Updates & Compliance Changes
Regulatory Requirements for Importers and Distributors of Medical Devices, EU MDR 2017/745
ISO 13485:2016
Mastering CAPA in the Medical Device Industry
The Medical Device Regulation (CE Marking Process Key Updates)
Understanding QMSR: Key Updates & Compliance Changes
Quality Systems and Regulations
Regulatory Requirements for Importers and Distributors of Medical Devices, EU MDR 2017/745
Duration:
1 day
Virtual Training:
£375
Dates & Location:
24 Sep 2026
Virtual
Overview
ISO 13485:2016 & The Medical Devices Regulation (CE Marking Process)
Duration:
2 days
In-Company training:
Customised
Live Virtual or On-Site training
Overview
Introduction to Life Sciences Manufacturing
Duration:
2 days
In-Company training:
Customised
Live Virtual or On-Site training
Overview
ISO 13485:2016
Duration:
1 day
Virtual Training:
£375
Dates & Location:
26 Oct 2026
Virtual
Overview
Mastering CAPA in the Pharmaceutical Industry
Duration:
2 days
In-Company training:
Customised
Live Virtual or On-Site training
Overview
Mastering CAPA in the Medical Device Industry
Duration:
2 days
Virtual Training:
£660
Dates & Location:
10 - 11 Nov 2026
Virtual
Overview
MDSAP: The Medical Device Single Audit Programme
Duration:
2 days
In-Company training:
Customised
Live Virtual or On-Site training
Overview
The Medical Device Regulation (CE Marking Process Key Updates)
Duration:
1 day
Virtual Training:
£375
Dates & Location:
27 Oct 2026
Virtual
Overview
Navigating Combination Product Regulations
Duration:
1 day
In-Company training:
Customised
Live Virtual or On-Site training
Overview
Understanding QMSR: Key Updates & Compliance Changes
Duration:
0.5 day
Virtual Training:
£225
Dates & Location:
13 Oct 2026
Virtual
Overview
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