GMP: FDA´s New Regulations for Drug Manufacturers
The US Food and Drug Administration (FDA) amends its requirements for foreign and domestic establishment registration and listing for human drugs, including drugs that are regulated under a biologics license application, and animal drugs. The final rule revises FDA\'s longstanding regulations governing drug establishment registration and drug listing. The amendments are aimed at modernizing these regulations and improving efficiency and reliability for both - FDA and drug manufacturers.
The source of the news: http://www.gmp-compliance.org/enews_05571_FDA%C2%B4s-New-Regulations-for-Drug-Manufacturers.html