A Comprehensive View of FDA Regulations for Medical Devices
Website https://www.complianceonline.com/fda-regulations-for-medical-devices-seminar-training-80118SEM-prdsm |
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Deadline: July 06, 2020 | Date: July 16, 2020-July 17, 2020
Venue/Country: Tampa, FL, U.S.A
Updated: 2020-05-09 00:02:56 (GMT+9)
Call For Papers - CFP
Don’t let a common misunderstanding get you into trouble! There is more to the US Medical Device Regulations than Part 820.Companies that don’t understand will face regulatory scrutiny and receive FDA Form 483s and Warning Letters. Recently a device manufacturer got a Warning Letter relating to updates to shipped devices, which said, “The Quality Manager stated he was unaware of the corrections and removal reporting and recordkeeping requirements.”Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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