Creating reports
Intland Software has been a regular exhibitor at MedConf for several years. This must-attend event for developers of healthcare technology provides a great platform to discuss challenges and best practices. This year, we used the occasion to introduce new products for medtech innovators!
Held between 23-24 Oct 2019 in Munich, Germany, MedConf boasted over 63 speakers with insightful talks to spark discussions about medical device software engineering and other health tech questions. Intland Software’s talk attracted an enthusiastic crowd and provided insights into tying in engineering and quality management.
In a highly successful talk titled Aligning QMS and Engineering Processes in Medical Product Development, Intland’s Quality and Regulatory Expert Szabolcs Agai talked about integrating the work of quality and regulatory teams. The talk preceded an even more exciting event: the launch of two new medical product development templates for our QMS + ALM platform Intland Retina!
Attendees got a chance to learn about Intland’s new Medical Software Engineering Template (for compliance with IEC 82304-1, IEC 62304, ISO 14971, and FDA 21 CFR Parts 11 & 820), and the all-new Medical Audit & CAPA Template (for ISO 13485:2016 and FDA Title 21 CFR Part 820 compliance). Targeted for use by medical device engineering and quality teams, these templates save time and costs in the delivery of quality health technology.
To learn about these new templates for Intland Retina, visit Intland’s blog: Introducing Intland’s New MedTech Development Templates
Thanks to all visitors who attended our talk and stopped by our booth to learn more about our new products! We hope that we were able to inspire you to find ways to develop better quality MedTech products faster. Don’t hesitate to reach out to us with any questions! We’re looking forward to seeing you next year at MedConf 2020.
Flick through the PPT of Szabolcs Agai’s talk at MedConf 2019 about Aligning QMS and Engineering Processes in Medical Product Development: