federal_register: 2017-23526
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
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| document_number | title | type | abstract | publication_date | pub_year | pub_month | html_url | pdf_url | agency_names | agency_ids | excerpts | regulation_id_numbers |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2017-23526 | Assessing User Fees Under the Generic Drug User Fee Amendments of 2017; Draft Guidance for Industry; Availability | Notice | The Food and Drug Administration (FDA or Agency) is announcing the availability of a draft guidance for industry entitled "Assessing User Fees Under the Generic Drug User Fee Amendments of 2017." This draft guidance provides stakeholders information regarding the implementation of the Generic Drug User Fee Amendments of 2017 (GDUFA II) and policies and procedures surrounding its application. | 2017-10-30 | 2017 | 10 | https://www.federalregister.gov/documents/2017/10/30/2017-23526/assessing-user-fees-under-the-generic-drug-user-fee-amendments-of-2017-draft-guidance-for-industry | https://www.govinfo.gov/content/pkg/FR-2017-10-30/pdf/2017-23526.pdf | Health and Human Services Department; Food and Drug Administration | 221,199 | The Food and Drug Administration (FDA or Agency) is announcing the availability of a draft guidance for industry entitled "Assessing User Fees Under the Generic Drug User Fee Amendments of 2017." This draft guidance provides stakeholders information... |