MedTech I.Q.

The Cutting Edge of Medical Technology Content, Community & Collaboration

Tougher Import Rules for FDA Imports in 2015 at San Diego, CA

Event Details

Tougher Import Rules for FDA Imports in 2015 at San Diego, CA

Time: July 16, 2015 at 9am to July 17, 2015 at 6pm
Location: DoubleTree by Hilton Hotel San Diego Downtown
Street: 1646 Front Street, San Diego, California, 92101, USA
City/Town: San Diego
Website or Map: https://www.globalcompliancep…
Phone: 18004479407
Event Type: clinical, food, fda, medical, device, defence, and, navy, aerospace, mining
Organized By: GlobalCompliancePanel
Latest Activity: Apr 22, 2015

Export to Outlook or iCal (.ics)

Event Description


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. 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.

Why you should attend:

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.

Who Will Benefit:
  • Domestic importers
  • Foreign exporter
  • Initial importers
  • International trade executives
  • Venture Capitalists
  • Marine insurance underwriters
  • Import Brokers
  • Regulatory affairs managers


Casper (Cap) Uldriks owns Encore Insight LLC, which provides consulting services on FDA Law. He 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. 

Location: San Diego, CA        Date: July 16th & 17th, 2015        Time: 9 AM to 5 PM 
 DoubleTree by Hilton Hotel San Diego Downtown

Venue Address: 1646 Front Street, San Diego, California, 92101, USA

Price: $1,295.00   (Seminar for One Delegate)

Register now and save $200. (Early Bird)

Until June 10, Early Bird Price: $1,295.00

From June 11 to July 15, Regular Price: $1,495.00

Contact Information:

NetZealous LLC,

DBA GlobalCompliancePanel

161 Mission Falls Lane,

Suite 216, Fremont, CA 94539, USA         

USA Phone: 800-447-9407

Fax: 302-288-6884  

Comment Wall


RSVP for Tougher Import Rules for FDA Imports in 2015 at San Diego, CA to add comments!

Join MedTech I.Q.

Attending (1)

© 2021   Created by CC-Conrad Clyburn-MedForeSight.   Powered by

Badges  |  Report an Issue  |  Terms of Service