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EAS Consulting Group - FDA Submission Assistance

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EAS Consulting Group - FDA Submission Assistance

The FDA has established a wide variety of product submission requirements across the pharma, device and other regulated segments.Whether you are seeking assistance with an ANDA, DMF, 510(k), GRAS/NDI or a color certification, EAS Consulting Group is a valuable partner in the development and execution of an effective regulatory filing plan to achieve a successful submission. Our team of experts will work with you throughout the product development and submissions life cycle to help you identify the regulatory requirements,assemble product dossiers, evaluate the studies and draft the required submissions documents to give your file the best advantage for successful review by the FDA. We can also assist in maintaining the required facility registrations and product listings as your U.S. Agent