Computer System Validation (10478)

GMP data exist in paper or electronic form, with the latter becoming more and more common. The reasons are obvious: due to the increasing amounts of data, a reasonable evaluation on paper is becoming increasingly difficult. In addition, all the compliance requirements, once set up, are much easier to handle in electronic form and with fewer staff. You just have to set it up once. And in this webinar you will learn how this can be done in a lean and simple way.

Further contents:

• Introduction into the world of CSV
• Lifecycle: Risk Management, Design & Initial Testing
• Lifecycle: operational phase, changes, decommissioning
• Future insights: Pharma4.0, Computer System Assurance

Duration: about 90 minutes
Presentation language: English | Slides: English

...more from your speaker Fritz Röder...

Webinars allow you to participate in training courses and lectures conveniently from anywhere at any time. They are the perfect way to keep up to date with the latest knowledge without much effort. You are also welcome to ask the speaker questions after the webinar.

Note on quota call-off: When booking this individual part described here, one part per trained person will be deducted.

For team trainings please contact us.