HBW Insight is part of Pharma Intelligence UK Limited

This site is operated by Pharma Intelligence UK Limited, a company registered in England and Wales with company number 13787459 whose registered office is 5 Howick Place, London SW1P 1WG. The Pharma Intelligence group is owned by Caerus Topco S.à r.l. and all copyright resides with the group.

This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

Printed By

UsernamePublicRestriction

HR 9 regulatory risk assessment would add $20 mil. to FDA spending, CBO estimates.

This article was originally published in The Rose Sheet

Executive Summary

REGULATORY RISK ASSESSMENT WOULD ADD ABOUT $20 MIL. TO FDA SPENDING on pre-market regulatory activities each year, the Congressional Budget Office estimates in scoring of the Commerce Committee version of HR 9, the "Job Creation and Wage Enhancement Act," released Feb. 15. The $20 mil. cost is based on "information from FDA," CBO said. Another $17.5 mil. would be added to the cost of rulemaking, FDA maintained. "The agency estimates that the additional analysis required by the bill would add an average of about $700,000 to an additional 25 rules each year," CBO said.

Latest Headlines
See All
UsernamePublicRestriction

Register

RS001343

Ask The Analyst

Ask the Analyst is free for subscribers.  Submit your question and one of our analysts will be in touch.

Your question has been successfully sent to the email address below and we will get back as soon as possible. my@email.address.

All fields are required.

Please make sure all fields are completed.

Please make sure you have filled out all fields

Please make sure you have filled out all fields

Please enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel