GlobalCompliancePanel proudly presents its upcoming In-Person seminar on "FDA's and the U.S. Customs Border Patrol's Import and Export Control Program"
FDA's and the Customs and Border Patrol Service (CBP) has 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.
- Los Angeles-Long Beach, CA (1888PressRelease) July 16, 2014 - A number of factors can derail the expectation of a seamless import process. The course covers detailed information about the roles and responsibilities of the various parties involved 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.
Reasons to Attend this Valuable Session:
What happens when your product is detained? FDA will begin a legal process that can become an expensive business debacle. You must respond fully within short timeframes. This is not the time for you to be on a learning curve. You need to have a plan in place and know what you are doing.
The FDA is steadily increasing the legal and prior notice information requirements. If you do not know what those requirements are and you initiate a shipment, your product is figuratively dead in the water. You must be accurate with the import coding information and understand the automated and human review process. If not, you can expect detained shipments.
What happens when FDA decides you should bring the products back to the port of entry after you received a release but you cannot locate the product that has been sold? CBP may fine you three times the value of the shipment. FDA may have other adverse legal concerns and strategies.
When products are refused, you have different options. Some options may cost more than others. For example, your product may be destroyed by the government. You may be fined if you do not act in a timely manner.
These are common problems that become prohibitively expensive. You should know how to avoid common problems or at least how to mitigate the cost by using established and effective business planning.
The List of Individuals for whom this Course will be benefited:
• Domestic importers
• Foreign exporter
• Initial importers
• International trade executives
• Venture Capitalists
• Marine insurance underwriters
• Import Brokers
• Regulatory affairs managers
• Import / Export consultants
• In-house counsel
• Contract specialists
• Logistics managers
• Third party establishment inspection entities
• Sales managers
• Investors
Meet your Expert:
Casper (Cap) Uldriks brings over 32 years of experience from the FDA. He specialized in the FDA's medical device program as a field investigator, served as a senior manager in the Office of Compliance and as an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements. He is recognized as an exceptional and energetic speaker. His comments are candid, straight forward and of practical value. He understands how FDA thinks, operates and where it is headed. Cap now works almost exclusively on medical device issues at Olsson, Frank and Weeda (OFW Law in Washington, D.C.
Date: August 21st & 22nd 2014 (9 AM to 6 PM EDT)
Location & Venue: DoubleTree by Hilton Hotel Los Angeles Downtown, Los Angeles, California, 90012, USA
For Registration, Click on the link below:
https://www.globalcompliancepanel.com/control/~product_id=900088SEMINAR
Call our representative TODAY on 1800 447 9407 to have your seats confirmed! Or Email us to support ( @ ) globalcompliancepanel dot com
Organizer:
GlobalCompliancePanel imparts knowledge of best practices in industry to guarantee effective implementation of compliance programs for meeting regulatory demands. The key focus of GlobalCompliancePanel is to provide extensive and quality training for risk management, regulatory compliances, corporate governance and quality management.
Our Achievements:
• Over 300 Experts that are Renowned in their Respective Areas
• Successfully Trained more than 20,000 Compliance Professionals
• A Most Comprehensive Portal for Trainings, Industry Updates and Professional Growth
• Having more than 2000 Online Courses
• Successfully Completed more than 170 Seminars in US and Globally
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