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Tuesday, February 24, 2015
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Webinar On Key Regulatory Documents: Design History File (DHF), Device Master Record (DMR), Device History Record (DHR) and Technical File (TF) and Design Dossier
February 24, 2015 from 1pm to 2:30pm – Online Description : There are key regulatory documents global medical device companies must meet for the U.S. and the European Union / Common Market. And there are important differences. The cGMPs mandate… Organized by Compliance Trainings | Type: webinar
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Webinar On Computerized System Validation: Basic Concepts
February 24, 2015 from 1pm to 2:30pm – Online Description : The basic concepts of computerized system validation originated in the 1960s, with the Department of Defense and NASA. Validation of systems became a growing issue within the pharmaceut… Organized by Compliance Trainings | Type: webinar
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