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ONLINE WEBINAR 2017 - Preparing a US FDA Medical Device 510(k) Submission and Deciding When to Submit a 510(k) for a Change to an Existing Device

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Category US FDA Medical Device, 510(k) Submission, 510(k) for a Change, Medical Device approval, FDA 510K recommendations, 510K requirements, device safety and effectiveness, device safety, QS regulation, CAPA, FDA review and approval, FDA 510K document.

Deadline: April 10, 2017 | Date: April 11, 2017

Venue/Country: CA, U.S.A

Updated: 2017-03-20 18:14:49 (GMT+9)

Call For Papers - CFP

Learn how to prepare an FDA Medical Device 510(k) Submission and when to Submit a 510(k) for a change to an existing device. Register for this training course.

Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.