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portada Medical Device Reporting - Electronic Submission Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
Type
Physical Book
Language
Inglés
Pages
62
Format
Paperback
Dimensions
25.4 x 17.8 x 0.3 cm
Weight
0.12 kg.
ISBN13
9781727519402

Medical Device Reporting - Electronic Submission Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition)

The Law Library (Author) · Createspace Independent Publishing Platform · Paperback

Medical Device Reporting - Electronic Submission Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - The Law Library

New Book

£ 21.46

  • Condition: New
Origin: U.S.A. (Import costs included in the price)
It will be shipped from our warehouse between Friday, July 26 and Friday, August 02.
You will receive it anywhere in United Kingdom between 1 and 3 business days after shipment.

Synopsis "Medical Device Reporting - Electronic Submission Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition)"

Medical Device Reporting - Electronic Submission Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition) The Law Library presents the complete text of the Medical Device Reporting - Electronic Submission Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition). Updated as of May 29, 2018 The Food and Drug Administration (FDA) is revising its postmarket medical device reporting regulation and making technical corrections. This final rule requires device manufacturers and importers to submit mandatory reports of individual medical device adverse events, also known as medical device reports (MDRs), to the Agency in an electronic format that FDA can process, review, and archive. Mandatory electronic reporting will improve the Agency's process for collecting and analyzing postmarket medical device adverse event information. Electronic reporting is also available to user facilities, but this rule permits user facilities to continue to submit written reports to FDA. This final rule also identifies changes to the content of required MDRs to reflect reprocessor information collected on the Form FDA 3500A as required by the Medical Device User Fee and Modernization Act of 2002 (MDUFMA). This book contains: - The complete text of the Medical Device Reporting - Electronic Submission Requirements (US Food and Drug Administration Regulation) (FDA) (2018 Edition) - A table of contents with the page number of each section

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