EAS provides assistance with submissions for all FDA industry products and facilities. Our scientific experts in areas such as toxicology, radiology, chemistry, microbiology, packaging and our in-depth knowledge of government laws and regulations, EAS consultants can lead your company through the process of obtaining necessary background data, pre-meetings with the Agency, preparation and filing of the submission and act as a conduit between the Agency and the sponsor during the review process. EAS is well known in the industry as the highest level of expertise and is routinely called upon for GRAS, NDI, DMF, IDEs and more.