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Wednesday, February 26, 2014
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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 26, 2014 from 12pm to 1pm – 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 compliancetrainings | Type: online, training
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Webinar On - Due-diligence and Gap Analysis in Decision Making Process for Medical Companies
February 26, 2014 from 12pm to 1pm – Online Webinar In this seminar, we will discuss practical decision making steps you can follow to analyze whether to transfer or invest in keeping production in-house from a successful case study. If it is decided… Organized by Compliance Trainings | Type: online, training
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