Former Senior FDA Official to Conduct Popular ComplianceOnline Seminar on the FDA’s Import Program

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ComplianceOnline, the leading GRC advisory network, and ex-FDA official, Casper Uldriks, will conduct a two day seminar on FDA’s import legal requirements and policies.

FDA's New Import Program for 2017 - Strict Precision

FDA's New Import Program for 2017 - Strict Precision

2-Day In-Person Seminar by Ex-FDA Official: FDA's New Import Program for 2017 - Strict Precision

After successful events in 2016, ComplianceOnline, the leading governance, risk and compliance advisory network with over 500 experts in various regulatory subjects, today announced that it will be conducting its popular seminar on FDA's New Import Program for 2017 - Strict Precision in Orlando, FL on March 9 and 10, 2017.

Ex-FDA official Casper Uldriks will once again be the seminar instructor, discussing FDA’s new cost-saving import programs and on how U.S. customs and FDA legal requirements intersect.

FDA’s regulatory controls for imported and exported devices have become increasingly pervasive and stringent. Foreign manufacturers, foreign exporters and domestic initial importers face greater scrutiny and are subject to expensive consequences if they do not plan carefully.

This seminar will offer attendees a broader perspective of FDA’s and the US Customs Border Patrol’s regulatory criteria, inter-agency agreements, and intra-agency procedures. The various sessions will also address managing foreign suppliers, FDA’s internal procedures, and best practices for mitigating and resolving import detentions.

Speaker Casper Uldriks has over 32 years of experience with 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 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 understands how FDA thinks, how it operates, and where it is headed. Based on his broad experience and knowledge, he can synthesize FDA’s domestic and international operational programs, institutional policy and thicket of legal variables into a coherent picture.

For more information or to register for the seminar, please click here.

Dates: Thursday, March 9, 2017 (8.30 AM- 4.30 PM) and Friday, March 10, 2017 (8.30 AM- 4.30 PM)
Location: Orlando, FL
Registration Cost: $1,999.00 per registration
Early bird discounts: For discounts on early registrations, please click here.
Register by phone: Please call our customer service specialists at +1-888-717-2436 or email to customercare(at)complianceonline(dot)com

For more information on ComplianceOnline or to browse through our trainings, please visit our website.

About ComplianceOnline

ComplianceOnline is a leading provider of regulatory compliance trainings for companies and professionals in regulated industries. ComplianceOnline has successfully trained over 35,000 professionals from 9,000 companies to comply with the requirements of regulatory agencies. ComplianceOnline is headquartered in Palo Alto, California and can be reached at http://www.complianceonline.com. ComplianceOnline is a MetricStream portal. MetricStream (http://www.metricstream.com) is a market leader in Enterprise-wide Governance, Risk, Compliance (GRC) and Quality Management Solutions for global corporations.

For more information please contact:

A Reuben Bernard
Associate Director - ComplianceOnline
2600 E Bayshore Rd
Palo Alto CA USA 94303
Phone - +1-650-238-9656 | +1-888-717-2436
Fax - 650-963-2556
Mail: reuben(at)complianceonline(dot)com
Website: http://www.complianceonline.com

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A Reuben Bernard
@Compliance_On
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