Woodcock Encourages Patient Groups To Take Lead To Speed Regulatory Process, Development

This article was originally published in The Pink Sheet Daily

11 Jul 2014
News

Sarah Karlin pinkeditor@informa.com

Executive Summary

Medical and patient communities can help make up for FDA’s resource gaps by developing PRO standards and benefit-risk frameworks for specific diseases, FDA drug chief says.

Already Registered? Sign in to continue reading.

New to Pink Sheet? Start a free trial today!

Table
View full table

Topics

United States

Related Companies

Alkermes PLC

ASK THE ANALYST
Email

Print
Bookmark
Share

Tags:

BioPharmaceutical North America United States

You must sign in to use this functionality

Authentication.SignIn.HeadSignInHeader

PS077429

Please Note: You can also Click below Link for Ask the Analyst
Ask The Analyst

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 enter a valid e-mail address

Please enter a valid Phone Number

Ask your question to our analysts

Cancel

PS077429

All set! This article has been sent to my@email.address.

All fields are required. For multiple recipients, separate email addresses with a semicolon.

Please Note: Only individuals with an active subscription will be able to access the full article. All other readers will be directed to the abstract and would need to subscribe.

Woodcock Encourages Patient Groups To Take Lead To Speed Regulatory Process, Development

News

Executive Summary

Related Content

20 Is The Loneliest Number: FDA Disease Meeting Schedule Leaves Some Worried About Exclusion

Topics

Related Companies

You must sign in to use this functionality

Authentication.SignIn.HeadSignInHeader

Register

Ask The Analyst

Email Article

Sign In To Set a Search Alert