Conference on Medical Device Software Tougher Regulation

October 20 – October 21, 2016
Location:
To Be Announced
Chicago, IL
Event Details:

FDA's and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of information and adherence to government procedures. Firm's that fail to understand and properly execute an import and export program find that their shipment is delayed, detained or refused. In 2016 entries must use the Automated Commercial Environment (ACE) entry filing system or face entry refusals and monetary penalties up to $10,000 per offense. A number of other factors can derail the expectation of a seamless import process. The course covers detailed information about the roles and responsibilities of the various parties with an import operation and how to correct the weakest link(s) in the commercial chain. The course will include tips on how to understand FDA's thinking and offer anecdotal examples of FDA's import program curiosities.

Host:
NetZealous DBA GlobalCompliancePanel

For More Information:
John Robinson
support@globalcompliancepanel.com

VIEW THE EVENT WEBSITE