[Free Seminar on September 29] QMS and Regulatory Submissions for SaMD and Software Medical Devices: Practical Guidance from Medical Device Determination to QMS Inspections

▤ Summary

Berry will host a free online seminar on September 29, 2026 about QMS and regulatory filing for SaMD and software medical devices. The session will cover how to determine whether software qualifies as a medical device, how to prepare regulatory submissions, and how to handle QMS conformity inspections. It will also introduce Berry’s cloud-based eQMS product, QMSmart, and show how it supports document control, CAPA, and training workflows. The event targets IT and software companies considering entry into the medical device market, as well as teams that manage quality and regulatory compliance.

▦ Linked Companies

Berry

up to $1M