EAS U.S. Agent, Import Assistance, Registration and Listing Services
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EAS Consulting Group provides registration and listing assistance as well as US Agent services to international clients in all FDA regulated areas. US Agents are required by FDA to act as an intermediary between foreign firms and FDA. By quickly responding to questions and concerns in a timely manner EAS helps clients get their compliant products to the US marketplace as quickly as possible. Choose EAS for:
- Establishment Registrations
- Drug Submissions (IND, DMF, ANDA, Amendments)
- Medical Device Applications and Correspondence (510(k), 513(g) PMA, IDEs, De Novo, Pre-Submission)
- Process Filing for Acidified and Low-Acid Canned Foods (LACF) & Establishment Registration
- Food Facility Registrations
- US Agent Services for Foreign Color Manufacturers Testing and Approval
- Preparation for FDA Inspections of Foreign Facilities
- Corrective Action Plans
- Assistance with FDA Import Requirements and Detained Product Clearance
