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FDA corrects contact information for the Expedited Investigational New Drug Pilot Program docket, which solicits public input on shortening timelines from drug identification to first-in-human clinical trials.
National Securities Clearing Corporation proposes enhancements to supplemental liquidity deposit rules, methodology, and processes for member firms.
The FDA seeks OMB clearance for information collection procedures related to premarket approval of medical devices under the Paperwork Reduction Act.
NYSE American amends its connectivity fee schedule for market data and trading access; the rule change is effective immediately.
NYSE Arca proposes amendments to its connectivity fee schedule, effective immediately upon SEC filing.
NYSE Texas, Inc. amends its connectivity fee schedule to adjust charges for market data and trading access services.
NYSE American modifies its options fee schedule for manual transactions, with changes effective immediately.
The Office of the Assistant Secretary for Health seeks public comments on a proposed threshold for scheduling 7-hydroxymitragynine under the Controlled Substances Act.
SEC proposes to extend the information collection requirements under Investment Company Act Rule 0-1 for defining terms applicable to registered investment companies; public comment deadline is 60 days from Federal Register publication.
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