MedTech Import/Export: Regulations, Procedures, Best Practices

Rules and procedures for import and export of medical devices are growing more so with new rules and with changes in international trade agreements. Customs and FDA have been requesting more information and conducting more inspections and examinations than before. Mistakes in procedures or documentation can lead to withheld or seized shipments and consequent financial lost to U.S. and foreign manufacturers, suppliers, and brokers. This one-day program with speakers from government, industry, and consulting firms will cover the laws and regulations, recent changes, procedures, best practices, and common mistakes. Registration will open soon.