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This webinar is intended for professionals engaged in the R&D, QA and RA of medical device software. The seminar will feature some of the most recent changes of regulations, guidance and standards.
The webinar presenters: Gadi Ginot, CEO, Physio-Logic; Keren Elghouzzi-Kazachinsky, Head of SwQA, Physio-Logic; Vladimir Zotov, Sr. RA & QA Expert, Physio-Logic
The presentations: July 2016 Revision of MEDDEV 2.1/6 on the Classification of Stand-alone Software as Medical Device; IEC 62304, Amendment 1:2015; 2016 US FDA Draft Guidance on Post-Market Management of Cybersecurity; Implementing Agile in the Medical Device Space in Compliance with US FDA and CE Expectation;

Time: 14 Nov, Monday, 11:00-12:00

registration: Your registration request for this webinar will be submitted for approval. You will receive information via email regarding your registration status. The organizers reserve the right to make changes.

About Physio-logic: the company provides a full synergetic solution to medical device companies in the fields of quality assurance, including software QA, regulatory affairs and clinical trials.