Extended impact assessment of a draft EC regulation on medicinal products for paediatric use [electronic resource] / Wija J. Oortwijn [and others]

The European Commission provides a structural solution to the lack of testing of medicinal products for the pediatric population. This report describes the economic, social, sustainable, and environmental impacts of a proposed regulation. The assessment indicates that the regulation will achieve its...

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Bibliographic Details
Online Access: Online Access
Corporate Author: RAND Europe
Other Authors: Oortwijn, W. J. (Editor)
Other title:Extended impact assessment of a draft European Commission regulation on medicinal products for paediatric use.
Format: Electronic eBook
Language:English
Published: Santa Monica, CA : RAND Corp., ©2004.
Series:RAND research brief (Online) ; MG-308-EC.
Subjects:
Description
Summary:The European Commission provides a structural solution to the lack of testing of medicinal products for the pediatric population. This report describes the economic, social, sustainable, and environmental impacts of a proposed regulation. The assessment indicates that the regulation will achieve its objectives, although the effects will vary.
Item Description:"MG-308-EC."
"RAND Europe."
"Prepared for the European Commission."
Physical Description:1 online resource.
Bibliography:Includes bibliographical references (pages 87-90)
Source of Description, Etc. Note:Title from title screen (viewed on March 27, 2005)