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avaFMEA
Digitalization of regulatory processes: How to start and what to consider

In this on-demand webinar, we will use practical examples from our projects to explain which questions you should ask yourself as early as possible, what needs to be decided when selecting a possible software solution, what you need to decide internally BEFORE starting a digitization project, and how you can ensure that, in the end, software is implemented that users are really happy with.

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avaPLMinterface
Post-Market Surveillance – Adverse Event Database Search

In this webinar, we will present you our new Polarion solution avaADVERSE, which was developed for a digitalized procedure for searches in adverse event databases and an automated interface to the FDA databases MAUDE and Recall. 

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avaRisk
Benefit Risk Determination for Medical Devices

This Tech-Talk explores the interface between risk management and clinical evaluation in medical devices. It covers topics like data exchange, traceability, and consistency between plans and reports, while addressing challenges in post-market surveillance and unresolved industry issues.

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avaFMEA
Computer Software Assurance for Medical Device QMS Processes

When a process is digitized with the help of a software, validation of the software is mandatory. This is required by ISO 13485 and also by the FDA in 21 CFR Part 820. However, there are significant differences in the concrete approach and the required effort.Therefore, it is crucial to have an appropriate software validation process established that allows flexibility for the different use scenarios. 

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avaUsability
Medical Device Development

It's no secret: One of the biggest challenges in product development are "silos" of information. They arise from processes that are not interlinked and specialist process teams that are not able to exchange information efficiently.

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avaPMCF
Post-Market Surveillance

Post-market Surveillance (PMS) is one of the most complex processes in medical device quality management systems due to its interface to many other processes. Get more Information in this TechTalk.

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Medical
Software Validation in the Medtech Industry

Software used for the support of processes in quality management systems (QMS) must be validated to confirm that the software fulfills the intended purpose. Important to understand is, that the validation must be conducted on the basis of the application process and in the IT environment of the software operator.

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AdobeStock_269860798
IMDRF Adverse Event Coding

Dieses Webinar gibt einen Überblick über die Coding Struktur und verwendete Kategorien von Terminologien. Darauf basierend wird erläutert, wie das Coding für verschiedene Prozesse des Qualitätsmanagementsystems angewendet wird.

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