| Literature DB >> 23946620 |
Abstract
Biosimilars, although not identical to their originator product, are expected to become essential in reducing health care costs and improving access to lifesaving drugs. The FDA must find a way to balance rigorous testing to ensure quality, as is done for generic chemical drugs, with providing a cost-efficient way to expedite approvals of these products.Year: 2013 PMID: 23946620 PMCID: PMC3737980
Source DB: PubMed Journal: P T ISSN: 1052-1372