federal_register: E6-21952
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| E6-21952 | Medical Device Regulations; Disqualification of a Clinical Investigator; Technical Amendment | Rule | The Food and Drug Administration (FDA) is amending a medical device regulation to include references to the Center for Biologics Evaluation and Research (CBER) and the Center for Drug Evaluation and Research (CDER). This regulation pertains to the disqualification of a clinical investigator. Currently, only a reference to the Center for Devices and Radiological Health is listed in this regulation. This action is being taken to ensure the accuracy of FDA's regulations. | 2006-12-22 | 2006 | 12 | https://www.federalregister.gov/documents/2006/12/22/E6-21952/medical-device-regulations-disqualification-of-a-clinical-investigator-technical-amendment | https://www.govinfo.gov/content/pkg/FR-2006-12-22/pdf/E6-21952.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA) is amending a medical device regulation to include references to the Center for Biologics Evaluation and Research (CBER) and the Center for Drug Evaluation and Research (CDER). This regulation pertains to the... |