| Literature DB >> 24980714 |
Federico M Goodsaid1, Felix W Frueh2.
Abstract
The FDA has developed a Pilot Process for Biomarker Qualification. Initial experience with this process has underscored the care that a long-term approach to biomarker qualification independently of development for specific drugs should have in the assembly of external industry consortia as well as the internal regulatory organization for these qualification efforts. There are complex scientific and clinical issues associated with these qualifications, and it is paramount that the expertise needed for their review be identified so that a comprehensive consensus may be reached at the end of this process. Several frequently asked questions associated with this process are presented in this paper, as well as answers reflecting the Agency's current thinking about this process.: © Published by Elsevier Ltd.Year: 2007 PMID: 24980714 DOI: 10.1016/j.ddtec.2007.10.005
Source DB: PubMed Journal: Drug Discov Today Technol ISSN: 1740-6749