Agency Information Collection Activities; Announcement of OMB Approval; Medical Device Reporting: Manufacturer Reporting, Importer Reporting, User Facility Reporting, and Distributor Reporting

ローカル自動翻訳 · 情報源の原言語

概要

The Food and Drug Administration (FDA) is announcing that a collection of information entitled "Medical Device Reporting: Manufacturer Reporting, Importer Reporting, User Facility Reporting, and Distributor Reporting" has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995.

情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →

Agency Information Collection Activities; Announcement of OMB Approval; Medical Device Reporting: Manufacturer Reporting, Importer Reporting, User Facility Reporting, and Distributor Reporting

Agency Information Collection Activities: Proposed Collection; Comment Request

Office of Management and Budget (OMB) に提出された情報収集活動; Food and Drug Administration (FDA) の提出書類の提出; Customer/Partner Customer Service Satisfaction Surveys に関するコメントの要求

Office of the National Coordinator for Health Information Technology; Health Information Technology Advisory Committee; エンタイントにそすにしたプログルにしたプログにプログを定义にしたプログに。