Pink Sheet 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

Ephedra hearings

This article was originally published in The Tan Sheet

Executive Summary

House Energy & Commerce Committee/Subcommittee on Oversight & Investigations plans second day of hearings on botanical July 24, following previously-announced July 23 session (1"The Tan Sheet" July 14, 2003, In Brief). Hearings will take place in room 2123 in the Rayburn office building...

You may also be interested in...



Metabolife execs subpoenaed

House Energy & Commerce Subcommittee on Oversight & Investigations authorizes issuance of three subpoenas to former and current Metabolife employees in 9-0 vote. During business meeting held July 10, Rep. Greg Walden (R-Ore.) noted that in response to hearing invitation letters sent to 13 individuals, three Metabolife witnesses "have sent written responses through their respective counsels declining the invitation to testify." Founder, co-owner and former president Michael Ellis, former president David Brown and current employee Daniel Rodriguez will be issued subpoenas "as quickly as possible," committee says. In response, Metabolife maintains it is cooperating with House investigation and "looks forward to having its senior officials, including" CEO Russell Schreck, testify. First of two hearings on ephedra is scheduled for July 23; House inquiry began in February (1"The Tan Sheet" March 3, 2003, p. 9)...

As Casgevy, Lyfgenia Launches Proceed, CRISPR And bluebird bio CEOs Reassure

The CEOs of bluebird bio and CRISPR Therapeutics hope to inspire investor confidence that their gene-based therapies for sickle cell disease and beta thalassemia will be widely reimbursed in the US and EU.

Japan Regulatory Update: Revised Law Widens RWD Scope, Price Revisions/Listings

Japan now allows pseudonymized personal data for medical use under a licensing system for wider use of real-world data. Meanwhile, a national cost-effectiveness assessment scheme has slashed reimbursement prices for Lagevrio and Kerendia, and Alexion’s Voydeya has been added to the reimbursement tariff.

Topics

Latest Headlines
See All
UsernamePublicRestriction

Register

PS095708

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