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An Online FDA and EU Technical Documentation Training Course: Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) - Earn up to 4.0 RAC Credits
17 janv. 2024 10h43 HE | Research and Markets
Dublin, Jan. 17, 2024 (GLOBE NEWSWIRE) -- The "Design History File (DHF), Device Master Record (DMR), and Device History Record (DHR) - A Technical Documentation Training" training has been added to...
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3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS
15 déc. 2023 06h13 HE | Research and Markets
Dublin, Dec. 15, 2023 (GLOBE NEWSWIRE) -- The "3-Hour Virtual Seminar on US FDA and EU Medical Device Directive Requirements for DHF, DMR, DHR and TF/DDS" webinar has been added to ...
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MedReg 2023: Annual Medical Device Regulatory Confex - Unveil the Future of Regulatory Compliance
16 août 2023 07h48 HE | Research and Markets
Dublin, Aug. 16, 2023 (GLOBE NEWSWIRE) -- The "MedReg 2023 - Annual Medical Device Regulatory Confex" training has been added to ResearchAndMarkets.com's offering. Step into the realm of...
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Avtec Inc. and Harris Corporation Announce New Strategic Alliance
22 mars 2017 19h03 HE | Avtec, Inc.
Highlights:  Avtec Inc. and Harris have agreed to work together and provide LMR customers with more choices in dispatch solutions  Avtec is the leading independent...
Locus Introduces Software to Automate NPDES Discharge Monitoring Reporting
20 mai 2013 07h00 HE | Locus Technologies
SAN FRANCISCO, CA--(Marketwired - May 20, 2013) - In response to industry and customer demands to streamline Discharge Monitoring Report (DMR) reporting under the National Pollutant Discharge...