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Held on February 20-21, 2020, in Vienna, Austria, this Summit shed light on classification, conformity assessment, and risk management in regulatory strategies to achieve compliance and ensure patients’ safety.
Through case studies, interactive presentations, and discussions, attendees learned which regulatory strategy is applicable for their products, how to develop effective tactics and how best to achieve smooth market access. Besides sharing best practices, this event offered a valuable opportunity for networking and partnering with businesses of diverse sizes and types.
The process of EU MDR Implementation can be complex and challenging, and our online Medical Devices: Regulatory and Compliance summit is here to help.
This two-day event will shed light on classification, conformity assessment, and risk management in regulatory strategies to achieve compliance and ensure patients’ safety. Through case studies, interactive presentations, and discussions, attendees will learn which regulatory strategy is applicable for their products, how to develop effective tactics, and how best to achieve smooth market access.