Events
Vialis offers a variety of events related to laboratory data systems. Here you will find a summary of our training courses, fairs, seminars or partner events
Wie mache ich mein Analytiklabor 21 CFR Part 11 tauglich?
Das Seminar erläutert die aktuellste regulatorische Sichtweise und Interpretation in Bezug auf computergestütze Systeme (u.a. 21 CFR Part 11, EU GMP Annex 11 Draft), erläutert die Vorgehensweise zur Implementierung von validierten Computersystemen – speziell auch in Bezug auf Neuerungen aus GAMP5 - und beschreibt unter anderem den Umgang mit 21 CFR Part 11 inkompatiblen Softwarelösungen aus praktischer Sicht. Die Aufrechterhaltung des validierten Zustands von Computersystemen und zugehöriges Change Management werden ebenfalls behandelt.
„Laborprozesse Papierlos gestalten“ – Von der Idee bis zur Umsetzung
Das Seminar gibt einen detaillierten Überblick über die modernsten Lösungen zur papierlosen Arbeitsweise in analytischen Laboratorien. Planung, technische Anforderungen und die Einführung regulatorisch kompatibler Lösungen basierend auf modernster LIMS-Technologie werden diskutiert und präsentiert. Dass es sich beim papierlosen Labor nicht um unerfüllte Träume handelt, wird anhand von Umsetzungsbeispielen aus der Praxis und Videos demonstriert.
How to Handle IT Systems in a Paperless Laboratory - 17-Sep-2013 in Stockholm, Sweden
Regardless of whether you have to comply with 21 CFR Part 11, ISO 9001, ISO 17025, or other requirements.
Course outline:
Don’t miss the opportunity to learn about IT compliance in a paperless lab. While 21 CFRF Part 11 is the pharmaceutical industry standard, there is little difference between these requirements and the requirements in e.g. ISO 17025, ISO 9001, and other standards. The goal is simply to have control over your IT systems and in a paperless lab this is even more important. This class teaches you how to be in compliance with the regulations.
How to Handle IT Systems in a Paperless Laboratory - 18-Sep-2013 in Eindhoven, The Netherlands
Regardless of whether you have to comply with 21 CFR Part 11, ISO 9001, ISO 17025, or other requirements.
Course outline:
Don’t miss the opportunity to learn about IT compliance in a paperless lab. While 21 CFRF Part 11 is the pharmaceutical industry standard, there is little difference between these requirements and the requirements in e.g. ISO 17025, ISO 9001, and other standards. The goal is simply to have control over your IT systems and in a paperless lab this is even more important. This class teaches you how to be in compliance with the regulations.
How to Handle IT Systems in a Paperless Laboratory - 19-Sep-2013 in Brussels, Belgium
Regardless of whether you have to comply with 21 CFR Part 11, ISO 9001, ISO 17025, or other requirements.
Course outline:
Don’t miss the opportunity to learn about IT compliance in a paperless lab. While 21 CFRF Part 11 is the pharmaceutical industry standard, there is little difference between these requirements and the requirements in e.g. ISO 17025, ISO 9001, and other standards. The goal is simply to have control over your IT systems and in a paperless lab this is even more important. This class teaches you how to be in compliance with the regulations.
Concept Heidelberg organizes “ Pharma Lab Congress”
Date: Wednesday, November 13 – Thursday, November 14 16:00, Düsseldorf, Germany
The PharmaLab Congress will cover various topics in 10 interesting conferences and lectures on analytics, paperless lab, bio analytics, microbiology and R&D.
More information and Registration here