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NeuroLogica Announces FDA 510(k) Clearance of BodyTom® 64

Legacy MEDSearch

a subsidiary of Samsung Electronics Co. Food and Drug Administration for commercial use in the United States. Director of Global Sales and Marketing of NeuroLogica. the healthcare subsidiary of Samsung Electronics Co., NeuroLogica Corp., About NeuroLogica. NeuroLogica Corp.,

FDA 92
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Pharmacovigilance deep dive: risk minimisation measures

European Pharmaceutical Review

An RMP is submitted as part of the dossier of all new drug applications and is evaluated by regulatory authorities before authorisation is given. Jouaville: Most RMM effectiveness studies are formatted as surveys or drug utilisation studies (DUS). US Food and Drug Administration. Available from: [link].

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Uri Goren

Cadensee

02:25 Uri Goren talks about his road to become a trailblazer and advocate for patient-centric healthcare. 21:40 At what scale is breaking away from traditional channel to market is happening on a wide scale in the industry? 52:21 Uri's opinion about the main problem that needs to be solved for the healthcare market with technology.