Change Country
×
SQT
SQT
-or-
Close this window
Download
×
I would like to receive updates on upcoming courses, including industry news and updates from SQT Training Ltd.
By clicking 'Download Now', you agree to our
privacy policy
+353 61 339040
info@sqt-training.com
Moodle Login
View reviews
Menu
Home
Courses
A-Z of Programmes
Lean Six Sigma, Process & Project Management
Lean Six Sigma
Join our Lean Six Sigma Network
Continual Process Improvement – Statistical Applications with Minitab
Project & Programme Management
Compliance, Standards & Auditing
Quality
Environment & Energy Management
Health & Safety
Laboratory
Integrated Management Systems
Sustainability
Information Security
Leadership & Personal Development
Leadership & Personal Development
Train the Trainer
Life Sciences – Medical Devices & Pharma
Quality Systems and Regulations
Validation
Risk Management
Testing and Calibration
Technical Writing
Internal Auditing
Cleanroom
GMP
Hospital & Medical
Food Safety
Food Safety Standards
Food Safety Auditing
HACCP & Food Safety Management Systems
Food Safety Training
Food Defence & Authenticity
Validation & Risk Management
PCQI
Close
In-Company Training
Virtual
News & Resources
News
Resources
Moodle login
Close
SQT Alumni
Close
About Us
About SQT
Why SQT?
Our Tutors
Accreditations
Close
Contact Us
Validation
Home
/
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:
£870
Dates & Location:
26 - 28 Nov 2024
Virtual
27 - 29 May 2025
Virtua
Overview
Software Validation
Duration:
3 days
Virtual Training:
£870
Dates & Location:
03 - 05 Dec 2024
Virtual
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:
£2,175 + £305 fees
Dates & Location:
29-30 Jan & 05-06 Feb & 26-27 March 2025
Virtual
Overview