lobbying_activities: 3000277
Data license: Public Domain (U.S. Government data) · Data source: Federal Register API & Regulations.gov API
This data as json
| id | filing_uuid | filing_type | registrant_name | registrant_id | client_name | filing_year | filing_period | issue_code | specific_issues | government_entities | income_amount | expense_amount | is_no_activity | is_termination | received_date |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 3000277 | cd957248-35fe-4fc7-822e-ebb4eb8b94b8 | Q2 | IPOLICY SOLUTIONS | 401105127 | INVITAE INC. | 2023 | second_quarter | MED | H.R.2369 - VALID Act of 2023 FDA Guidance, Docket No. FDA-2022-D-2983 for Considerations for the Design and Conduct of Externally Controlled Trials for Drug and Biological Products FDA public meeting, FDA-2018-N-4002 Electronic Submission of Adverse Event Reports to FAERS Using ICH E2B(R3) Standards FDA guidance, Docket No. FDA-2023-D-0110: Clinical Trial Considerations to Support Accelerated Approval of Oncology Therapeutics | Food & Drug Administration (FDA),HOUSE OF REPRESENTATIVES,SENATE | 90000 | 0 | 0 | 2023-07-10T10:03:38-04:00 |