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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
Medical Device FDA QSR & QSIT
ISO 13485:2016
CAPA for the Medical Device Industry
The Medical Device Regulation (CE Marking Process Key Updates)
ISO 13485:2016 & The Medical Devices Regulation (CE Marking Process)
Medical Device FDA QSR & QSIT
Pharma and Medical Device Industry – Introduction
ISO 13485:2016
CAPA for the Pharmaceutical Industry
CAPA for the Medical Device Industry
MDSAP: The Medical Device Single Audit Programme
The Medical Device Regulation (CE Marking Process Key Updates)
Regulations and Requirements for Combination Products
Medical Device FDA QSR & QSIT
ISO 13485:2016
CAPA for the Medical Device Industry
The Medical Device Regulation (CE Marking Process Key Updates)
Quality Systems and Regulations
ISO 13485:2016 & The Medical Devices Regulation (CE Marking Process)
Duration:
2 days
In-Company training:
Customised
Live Virtual or On-Site training
Overview
Medical Device FDA QSR & QSIT
Duration:
2 days
Virtual Training:
£695
Dates & Location:
26 - 27 May 2025
Virtual
Overview
Pharma and Medical Device Industry – Introduction
Duration:
2 days
In-Company training:
Customised
Live Virtual or On-Site training
Overview
ISO 13485:2016
Duration:
1 day
Virtual Training:
£345
Dates & Location:
10 Mar 2025
Virtual
Overview
CAPA for the Pharmaceutical Industry
Duration:
2 days
In-Company training:
Customised
Live Virtual or On-Site training
Overview
CAPA for the Medical Device Industry
Duration:
2 days
Virtual Training:
£605
Dates & Location:
18 - 19 Feb 2025
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:
£345
Dates & Location:
11 Mar 2025
Virtual
Overview
Regulations and Requirements for Combination Products
Duration:
1 day
In-Company training:
Customised
Live Virtual or On-Site training
Overview
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