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MDS
Project management and compliance made easy

Discover how to overcome complex challenges in medical technology with Teamcenter Medical Device Solution. Optimize team collaboration, streamline project management, and enhance product development. Join our webinar to learn proven strategies for efficiency and success. 

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avaClinical
Trends for digitalized Clinical Evaluation Documentation: Integration of SOTA & Claim Management

In this webinar we will introduce you to the new features in avaClinical 2.0 and their benefits.

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avaMedical_AdobeStock_325786162
Getting Started with Digitalized Medical Device Development: avaMedical

In this webinar find out more on how avasis and their Polarion products can help you implementing state-of-the-art digitalized processes in the medtech industry. 

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avaRegulatory
Regulatory Information Management

This on-demand webinar highlights efficient regulatory information management, integrating data into Polarion with avaREGULATORY, and guiding your company to prepare for upcoming changes through SMART standards.

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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

A huge problem in the MedTech industry: The 𝗶𝗻𝘁𝗲𝗿𝗳𝗮𝗰𝗲 𝗯𝗲𝘁𝘄𝗲𝗲𝗻 𝗰𝗹𝗶𝗻𝗶𝗰𝗮𝗹 𝗲𝘃𝗮𝗹𝘂𝗮𝘁𝗶𝗼𝗻 & 𝗿𝗶𝘀𝗸 𝗺𝗮𝗻𝗮𝗴𝗲𝗺𝗲𝗻𝘁 𝗳𝗶𝗹𝗲, and in particular the 𝗯𝗲𝗻𝗲𝗳𝗶𝘁-𝗿𝗶𝘀𝗸 𝗱𝗲𝘁𝗲𝗿𝗺𝗶𝗻𝗮𝘁𝗶𝗼𝗻 section in the clinical evaluation report. We strive to bring more clarity into that topic and help you understand current struggles of medical device manufacturers and how you can handle those.

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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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