Customs – Trade Partnership Against Terrorism (C-TPAT) and Supply Chain Security

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The Customs-Trade Partnership Against Terrorism (C-TPAT) is a voluntary supply chain security program led by U.S. Customs and Border Protection (CBP). It is intended to improve the security of supply chains of private enterprises against the threat of terrorism.

The program was launched in November 2001, with seven large U.S. companies as the initial participants. By the end of 2014, more than 10,000 members joined the effort. More than 4300 importers in the program account for more than half of the value of all merchandise imported into the U.S.

C-TPAT certification can be attained by companies who seek to be considered low risk, enabling their cargo to be processed in an expedited manner with fewer Customs examinations. The certification involves a documented process for determining and mitigating risk throughout a company’s international supply chain.

The program is voluntary, but affords those participating in it a huge advantage in terms of international trade. In this webinar, we will explore the best approach to C-TPAT certification and discuss best practices.

Areas Covered in the Session :

  • U.S. Customs and Border Patrol
  • C-TPAT Strategy
  • C-TPAT Certification and Benefits
  • International Terrorism
  • Mitigation of Terrorist Threats
  • Mutual Recognition Arrangements
  • Best Practices
  • Interactive Q&A Session
Who Will Benefit:

  • Supply Chain Departments
  • Quality Assurance Departments
  • Regulatory Affairs Departments
  • Legal Professionals in Manufacturing Companies
  • Information Technology Departments
  • Compliance Departments
  • Business Stakeholders responsible for manufacturing supply chain functions
  • Consultants working in the manufacturing/supply chain sectors of industry
  • Transportation personnel who are handling goods and supervisors
  • Security personnel responsible for supply chain activities
  • Auditors and Inspectors responsible for evaluating supply chain security and compliance

TL2049

Carolyn Troiano

Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated industries. She is currently an independent consultant, advising companies on computer system validation and large-scale IT system implementation projects.

During her career, Carolyn worked directly, or on a consulting basis, for many of the larger pharmaceutical companies in the US and Europe. She developed validation programs and strategies back in the mid-1980s, when the first FDA guidebook was published on the subject, and collaborated with FDA and other industry representatives on 21 CFR Part 11, the FDA’s electronic record/electronic signature regulation.

Carolyn has participated in industry conferences. She is currently active in the PMI, AITP, and RichTech, and volunteers for the PMI’s Educational Fund as a project management instructor for non-profit organizations.

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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance
.