In October, the second Polarion Major Release 2022 will be released. As always, our team is in the starting blocks to thoroughly check all changes and prepare the most important information for you. Sven Wittorf will show you the most important and helpful improvements of the new Polarion version in a webinar on 3 November 2022 at 11 am.

Sven Wittorf will address the following questions:

• Which new functions have been added?
• How are the functions to be assessed from the perspective of regulation in medical technology – do they make compliant work easier or more difficult?
• Which use cases can be implemented better with the new functions or at all?
• What needs to be considered when updating to this version?
• What is the impact on Medsoto’s tools?

The webinar will take place on Thursday, 3 November at 11 am and is free of charge. Of course, our team will answer your questions about the new version in the chat. We look forward to an exciting webinar with you!

At this event, Christian Johner and Andrea Seeck from the Johner Institute and Sven Wittorf from Medsoto GmbH will address the digital red thread in quality and regulatory affairs management for manufacturers of medical technology and products.

Registration Siemens Life Science Forums.

The focus is on the continuous data flow and the consistency and traceability of information and documents. Christian Johner opens the event with the contribution “Digitalisation and monitoring of standards” from the Johner Institute. Andrea Seeck picks up the thread and shows how the automated monitoring of regulations helps to ensure compliant products and processes. Sven Wittorf links this digital QM/RA thread with practical experience from R&D in his contribution “Integrating regulatory requirements into the development process”.

Finally, there will be enough time for questions.

Agenda

15:00-15:15: Welcome address
15:15-15:45: Impulse Talk “Digital transformation of regulatory processes” – Prof. Dr. Johner 15:45-16:15: Industry Talk “Automated monitoring of regulations ensure compliant products and processes” – Dr. Andrea Seeck, Johner Institute
16:15-16:45: TechTalk “Integrating regulatory requirements into the development process” – Sven Wittorf, Medsoto GmbH
16:45-17:00: Discussion & Questions