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Software testing is a required activity in the medical device industry. Regulatory requirements and the risk of injury to the patient, user, and environment make this a mandatory and highly scrutinized task. While the basic software testing process and techniques apply, there are definite differences. Through this webinar you will obtain an overview of the key FDA and International regulations that make software testing in the medical device space different than other industries.
To access the webinar recording of “How Software Testing is Different for Medical Device Software,” simply submit the form below.
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See the "5 reasons you should only register for ISTQB exams through ASTQB."