Principles of Computer Systems Validation (CSV) course
Help you meet regulatory requirements and mitigate risks to product quality and patient safety
Principles of Computer Systems Validation (CSV)
Description
Businesses can no longer operate without a level of reliance on computer systems. New technology and the industry hot topic “data integrity” (“information availability, authenticity, correctness and traceability”) are driving greater adoption of computerised information systems.
In response, regulators like the MHRA, TGA, FDA and Medsafe are increasingly scrutinising the validation of computer systems. As such, you must apply an appropriate level of risk-focused validation effort for your computer systems and organisation to be compliant.
The Computer Software Assurance (CSA) approach is being widely discussed for its use of critical thinking and risk assessment.
SeerPharma (UK) are pleased to bring the learning from Asia-Pacific’s leader in Quality Assurance and GMP solutions to the UK. The course runs over two days, three hours each morning. Your instructor will be Ian Lucas, Partner & Customer Solutions Business Manager from SeerPharma.
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Format and Course Length
The course will be delivered as an online virtual-classroom training session.
The training will be delivered as 2 x 3.5 hour sessions over 2 days. Each session will include a break. Participants to join at 8.45am in advance of a 9.00am start to test user’s technical issues
Participants will be provided with a PDF of the training material in advance of the training should they wish to print and annotate notes. Participants will be connected to the trainer and other participants via online collaboration tool Zoom with connected video (webcam / screen sharing) and audio (computer audio or phone dial-in). Theory will be delivered by the trainer sharing their screen of the PowerPoint presentation. Facilitated workshops will be run in digital breakout rooms (e.g. a group of 12 might split into 4 breakout rooms each with 3 participants to separately work on a problem). Breakout rooms can call the trainer in for support when required and the trainer can electronically bring everyone back to the main session to debrief when appropriate.
Participant needs are very basic. You will need a computer or suitable device with a good internet connection. A headset (headphones with microphone) and second monitor/screen are recommended but not required.
PDF Certificates will be provided to participants electronically.
Course Objectives
This course will provide you with an overview of what matters in validation of computerised systems (including CSA) to help your company meet regulatory requirements and mitigate risks to product quality and patient safety.
Through this course you will develop an:
- Understanding of common terms and definitions of Computer Systems Validation
- Understanding of the types of, and elements of System Development Life Cycles (SDLC)
- Understanding of Good Automated Manufacturing Practices (GAMP)
- Understanding of what is critical for data integrity in the eyes of GxP regulators
- Understanding of how computer systems are regulated in PIC/S (e.g. MHRA, TGA and Medsafe) and FDA environments
- Ability to recognise the compliance, risk, and regulatory consequences of using computer systems
Training audience
You will benefit from this course if you are a key Quality, IT or Operational Subject Matter Expert (SME) or Manager likely to be involved in using, validating, approving or purchasing computer systems.
Outside the UK? Contact Debra.Stanfield@seerpharma.co.uk for a VAT-free invoice