{"database": "openregs", "table": "dockets", "rows": [["FDA-2003-D-0433", "FDA", "International Cooperation on Harmonization of Technical Requirements for Registration of Veterinary Medicinal Products (VICH); Draft Guidance for Industry on Studies to evaluate the safety of residues of Veterinary Drugs in Human Food:  General Approach to Establish a Microbiological ADI (VICH GL-36) Request for Comments; Availability", "Nonrulemaking", "2021-09-01T01:03:21Z", "0b000064804a2308"]], "columns": ["id", "agency_id", "title", "docket_type", "last_modified", "object_id"], "primary_keys": ["id"], "primary_key_values": ["FDA-2003-D-0433"], "units": {}, "query_ms": 0.34812401281669736, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}