Seminar "Compute­rized Systems Validation (CSV)"

Cheerful People Listening to a Seminar
How to validate your compute­rized systems in an audit-proof manner and without unnecessary effort
Cheerful People Listening to a Seminar
How to validate your compute­rized systems in an audit-proof manner and without unnecessary effort

In this seminar, you will learn how to validate your computerized systems (e.g., ERP, compilers, or self-developed EOL testers) in a risk-based, fast, and regulatory-compliant manner and how to create the necessary documents so that you can confidently face future audits.

Registration for the seminar Computerized Systems Validation (CSV)

After your registration you will directly receive a booking confirmation with further details. After the confirmation you are bindingly registered, but you can name another person as a substitute at any time.

Seminar details

Computerized Systems Validation (CSV)
05.11.2025 from 09:00 until 17:00 o'clock
Online Seminar
German
680
809.2
Need help with registration? Please feel free to contact us at [email protected].

Contact person

Mr.
Mrs.
Divers

Participant

Mr.
Mrs.
Divers

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Do you have any further questions? Would you like another appointment or consider an In-house seminar? Get in touch with us!

Get a compact over­view of the require­ments for the CSV process

You will first learn about the regu­la­tory require­ments of ISO 13485:2016 and 21 CFR part 820 for validating computerized systems. We then illustrate the implemen­tation of suggestions from various guidance documents for fulfilling these require­ments using an exemplary CSV process based on ISO/TR 80002-2, which you can incor­porate directly into your quality management system after the seminar.

99% of participants recommend this seminar!

I really enjoyed the seminar. The scope was good, and everything was covered. I also liked the practical examples. The presentation and additional documents will definitely help me improve our company's procedures. Thank you very much!

seminar participant

Limit your validation efforts to the right level right from the start

After the seminar, you will know:

  • which systems require vali­dation and when revalidation is necessary. 
  • how IQ, OQ, and PQ interact. 
  • how a risk-based approach can limit the effort involved. 
  • what content and elements a validation plan contains. 
  • which methods can be used for testing and validation. 
  • how to achieve lean documen­tation of the validation results.

Put what you've learned directly into practice – thanks to concrete examples and tips

During the seminar, our expert will show you how to apply CSV using con­crete validation docu­ments from projects that have already been comple­ted. You will also benefit from useful, practical tips and learn about typical prob­lems that arise during audits and how to avoid them.

Certificate

There is a voluntary online exam at the end of the seminar (duration: approx. 20 min). By passing this exam, you will receive a certificate proving your newly acquired knowledge and skills in addition to your attendance confirmation.

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Further Information

Learning Content

The seminar covers the following topics: 

  • Definition of terms 
  • Regulatory requirements 
  • CSV procedure 
  • CSV validation assessment 
  • CSV and risk management 
  • Validation plan 
  • Test specification 
  • Validation performance and documentation 
  • Best practices
Learning Objectives

After the seminar, you will be able to:   

  • correctly assign and apply the definitions and terms related to the validation of computerized systems and the regulatory requirements from ISO 13485 and 21 CFR Part 820. 
  • evaluate computerized systems, determine requirements, and perform risk analyses in accordance with CSV. 
  • create validation and test plans. 
  • review CSV documentation. 
  • perform validation tests and document them appropriately. 
  • create validation reports.
Target Group

This seminar is designed for individuals who 

  • are required to validate computerized systems in medical technology companies. 
  • are required to review validation documentation (Quality Assurance Managers). 
  • operate computerized systems in medical technology companies and support Quality Assurance Managers in the validation of computerized systems (IT Specialists)
Requirements for Participation

The seminar is designed as a beginner's course for participants who have no experience with CSV and need to learn the basics (terms, activities).

What happens after registration?

After registering, you will receive a confirmation email containing the meeting link, the time, and information about the participants.  

An invoice will be sent to you within the next 48 hours, with a payment term of 14 days. If this payment term is not feasible for your company, please send a short e-mail to [email protected] to find a solution.  

Three days before our online seminars and workshops, you will receive two e-mails: The first contains the final link to the seminar and the second contains the access data to a cloud folder in which you will find documents for preparation, exercises, and presentations.   

If the seminar or workshop takes place in person, you will also receive the access link to your seminar documents three days before the date of the event. We will also provide documents in digital form for in-person events.

How is the seminar conducted?

The seminar takes place either in person or online.  

Our online/remote seminars and workshops are conducted via the video conferencing tool MS Teams. We recommend dialing in 20 minutes before the seminar begins so that any technical problems can be resolved in good time. If you have any questions or encounter any issues, our team is always available to help. 

We also recommend that you arrive at the seminar room approximately 20 minutes before the start of the face-to-face events.

At the end of the seminar, you will receive a feedback link for evaluation. The following day, we will send you your certificate of attendance.

What happens if questions or problems arise?

If you experience technical problems while participating or have any other questions, you can contact our support team anytime, even at short notice. The documents provided also include an emergency number to help you in urgent cases. 

Our general FAQ section answers further technical and organizational questions.

Get to know your trainer

Trainer Urs Mueller

Urs Müller works as a consultant at the Swiss Johner office and supports customers and projects in product development and the development of production equipment for medical technology, focusing on verification, validation (CSV), and software develop­ment. Since completing his computer science degree, Urs has worked in the software development service sector, first as a test automation engineer/tester and later as a team leader in an engineering company focusing on medical device development. Quality-driven development is in Urs' blood, and he enjoys sharing his enthusiasm for it with colleagues and customers. 

Inconvenient timing? Here, you will find further dates for this seminar:

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This seminar can also be booked as an in-house seminar

We are also happy to offer our seminars, courses, and workshops in-house. Depending on your needs, these can be held online or at your premises.

Please feel free to contact us​​​​​​​.

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