What kind of regulatory experience does Forest have?
Our regulatory expertise is a primary reason for our ability to bring products to market quickly and efficiently. Having brought several innovative drugs through the complex regulatory process, we have a commanding knowledge of relevant laws and regulations regarding Investigational New Drug/New Drug Applications (IND/NDA) and Quality Assurance/Quality Control (QA/QC) processes. Our track record includes meeting the requirements of the expedited review process for drugs such as Namenda.