documents: FDA-1995-D-0288-0027
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| id | agency_id | docket_id | title | document_type | subtype | posted_date | posted_year | posted_month | comment_start_date | comment_end_date | last_modified | fr_doc_num | open_for_comment | withdrawn | object_id |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| FDA-1995-D-0288-0027 | FDA | FDA-1995-D-0288 | 25 Reference 24 - ICH Harmonised Tripartite Guideline The Common Technical Document for the Registration of Pharmaceuticals for Human Use Quality M4Q(R1) re Chemistry, Manufacturing, and Controls Changes to an Approved Application: Certain Biological Products Draft Guidance for Industry | Supporting & Related Material | Background Material | 2017-12-22T05:00:00Z | 2017 | 12 | 2017-12-22T16:42:35Z | 0 | 0 | 0900006482d58787 |
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- 0 rows from regs_document_id in fr_regs_crossref