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Validation
Home
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Life Sciences - Medical Devices & Pharma
/ Validation
Public Programmes
In-Company Programmes
Process Validation & Equipment Validation
Software Validation
Process Validation for Medical Device Manufacturing – QQI Level 7
Process Validation & Equipment Validation
Software Validation
21 CFR Part 11 Electronic Records and Electronic Signatures
Fundamentals of Sterilisation Validation for Single Use Medical Devices
Validation of Software as a Medical Device and EN IEC 62304
Medical Device Usability
and EN IEC 62366
Process Validation for Medical Device Manufacturing – QQI Level 7
Process Validation & Equipment Validation
Software Validation
Process Validation for Medical Device Manufacturing – QQI Level 7
Validation
Process Validation & Equipment Validation
Duration:
3 days
Virtual Training:
€995
Dates & Location:
27 - 29 May 2025
Virtua
Overview
Software Validation
Duration:
3 days
Virtual Training:
€995
Dates & Location:
04 - 06 Mar 2025
Virtual
Overview
21 CFR Part 11 Electronic Records and Electronic Signatures
Duration:
1 day
In-Company training:
Customised
Live Virtual or On-Site training
Overview
Fundamentals of Sterilisation Validation for Single Use Medical Devices
Duration:
1 day
In-Company training:
Customised
Live Virtual or On-Site training
Overview
Validation of Software as a Medical Device and EN IEC 62304
Duration:
2 days
In-Company training:
Customised
Live Virtual or On-Site training
Overview
Medical Device Usability
and EN IEC 62366
Duration:
1 day
In-Company training:
Customised
Live Virtual or On-Site training
Overview
Process Validation for Medical Device Manufacturing – QQI Level 7
Duration:
6 days
Virtual Training:
€2,495 + €350 fees
Dates & Location:
29-30 Jan & 05-06 Feb & 26-27 March 2025
Virtual
Overview
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