Introduction to Quality and Regulatory aspects of Medical Devices Reports šŸ—“

On Saturday, 3rd October 2020, a webinar on Introduction to Quality and Regulatory Aspects of Medical Devices was conducted by the Department of BioMedical Engineering UCE, OU in association with IEEE OUCE EMBS Student Branch Chapter through Google meet platform. The webinar started from 6:15 pm and ended at 7:30 pm by Mrs. Samatha Gaddam, Regulatory Affairs Manager Global Medical Company Alcon USA. The event started by briefing about medical devices and different career options related to the medical device industry. There was a huge response from the students of Osmania University and BVRIT. Mrs. Samatha Gaddam discussed about active and non-active medical devices, global quality standards, classification of medical devices, aspects related to quality system, stages of product development. There was an interactive session between the speaker and the students throughout the whole event. At last, the webinar concluded by providing all the attendants Participation certificates. This webinar enlightened the participants and gave a comprehensive overview of Quality And Regulatory Aspects Of Medical Devices Speaker’s Profile Mrs. Samatha Gaddam is currently working as the Regulatory Affairs Manager in Global RA, Research team, in the Global Medical Company Alcon. She holds her international degrees in M.Sc in Biomedical Engineering, University of Iowa, USA. She was the Lead Developer in the Informatics Technology Service Sector and also gained experience as a research assistant. She then continued her career as a product specialist, Technical Auditor for MDD and AIMD in TUV SUD America, INC.

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