federal_register: 2013-27233
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| document_number | title | type | abstract | publication_date | pub_year | pub_month | html_url | pdf_url | agency_names | agency_ids | excerpts |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 2013-27233 | Medical Device Development Tools; Draft Guidance for Industry, Tool Developers, and Food and Drug Administration Staff; Availability | Notice | The Food and Drug Administration (FDA) is announcing the availability of the draft guidance entitled "Medical Device Development Tools." This document provides guidance to FDA staff, industry, healthcare providers, researchers, and patient and consumer groups on a new voluntary process within the Center for Devices and Radiological Health (CDRH) for qualification of medical device development tools (MDDT) for use in device development and evaluation programs. This draft guidance is not final nor is it in effect at this time. | 2013-11-14 | 2013 | 11 | https://www.federalregister.gov/documents/2013/11/14/2013-27233/medical-device-development-tools-draft-guidance-for-industry-tool-developers-and-food-and-drug | https://www.govinfo.gov/content/pkg/FR-2013-11-14/pdf/2013-27233.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA) is announcing the availability of the draft guidance entitled "Medical Device Development Tools." This document provides guidance to FDA staff, industry, healthcare providers, researchers, and patient and consumer... |