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...
Saved in:
Online Access: |
Online Access |
---|---|
Corporate Author: | |
Other Authors: | |
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: |
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) |