avaRIMx: Your Submission Management at a glance

Medical device and in vitro diagnostics (IVD) companies face rising regulatory requirements, complex approval processes and growing pressure to handle regulatory information reliably and efficiently.

Many teams still work with fragmented systems, manual processes and inconsistent data, making it difficult to maintain clear and up-to-date view of global requirements and product portfolios.

In this webinar, avasis Group and Siemens Digital Industries Software will show you the role of Regulatory Information Management within a modern digital enterprise landscape.

Through an interactive interview and live demonstration of avaRIMx, available on the Siemens Xcelerator platform, participants will see how Regulatory Affairs teams can gain visibility into product registrations, submission status, approval timelines, renewals and global regulatory activities to make well-informed decisions across global markets.

Whether you lead Regulatory Affairs, manage product data or oversee compliance and product portfolios, this webinar provides you insights into how digital regulatory management can improve visibility, control and efficiency.

Date: 15th of October 2026
Time: 10:00 CET
Duration: 60 minutes, including Live Q&A
Format: Online Webinar
Language: German with English subtitles

What You Will Learn:

• How to gain full visibility into product registrations, submission status, approval timelines, renewals and regulatory activities across global markets. 
• How avaRIMx helps manage submissions, responsibilities, tasks and deadlines in a single system. 
• How Regulatory Information Management fits into a broader digital enterprise strategy for medical device and IVD manufacturers. 
• How improved transparency, collaboration and data quality can help reduce manual effort and increase process efficiency. 

Who should participate?

This webinar is intended for professionals involved in regulatory operations, product compliance and digital transformation within the medical device and IVD industry:

• Regulatory Affairs Managers and Specialists responsible for submissions, registrations, renewals and regulatory workflows. 
• Regulatory Operations and Regulatory Excellence teams seeking greater visibility into regulatory status, deadlines and product approvals. 
• Management and executive decision-makers looking for greater transparency across product portfolios, market approvals and regulatory activities. 
• Quality and Compliance professionals responsible for maintaining regulatory oversight, traceability and process consistency. 
• Medical device and IVD manufacturers aiming to improve collaboration, reduce manual effort and standardize regulatory processes across global markets. 

Join us to see how avaRIMx and Siemens Digital Industries Software support a connected digital approach to Regulatory Affairs and Product Lifecycle Management, enabling greater visibility, efficiency and control across regulatory data, submissions and approvals.