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Customs and Trade Partnership Against Terrorism (C-TPAT) Certification and Compliance
- C-TPAT program overview and tier strategy
- Benefits of joining C-TPAT at a variety of levels
- Supply chain management, counterfeit and contraband activities
- Security for supply chain management
- Industry Pitfalls and Best Practices
- Q&A
Overview of the webinar
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.
In this webinar, we will provide an overview of the Customs and Trade Partnership Against Terrorism, C-TPAT program overview including “Tiered” strategy Program guidelines and highlights and C-TPAT compliance.
Who should attend?
- Supply Chain Management and Analysts
- Quality Assurance Management and Analysts
- Regulatory Affairs Management and Analysts
- Legal Professionals in Manufacturing Companies
- Information Technology Managers and Analysts
- Compliance Managers and Analysts
- 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
Why should you attend?
You should attend this training if you have a role in a manufacturing or freight/shipping company that handles goods distributed globally. The training will help you secure the international supply chain and mitigate the risks associated with illegal activities that support and fund terrorism.
Typically, anyone who is involved in securing the supply chain can benefit, whether handling goods physically or having an impact on the supply chain through policies, procedures, legal action or any other means.
This course will also help those in the CBP and related agencies who must understand the best practices suggested to aid in securing their global supply chains.
Faculty - Ms.Carolyn Troiano
Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health and other FDA-regulated industries. She is currently managing a large, complex data migration, analytics and reporting program at a major financial institution.
During her career, Carolyn worked directly, or as a consultant, for many top-tier pharmaceutical companies in the US and Europe. She was responsible for computer system validation across all GxP functions at a major pharmaceutical company. Carolyn developed validation programs and strategies back in the mid-1980s, when FDA guidelines were first issued. She was an industry reviewer for 21 CFR Part 11, the FDA's electronic record/electronic signature (ER/ES) regulation. She has taught ER/ES compliance, along with computer system validation and risk management/compliance at a number of Fortune 100 firms. Her experience includes work with FDA-regulated systems used in all areas of research, development, manufacturing, quality testing and distribution.
Carolyn has participated in industry conferences, providing very creative and interactive presentations. She is currently active in the Association of Information Technology Professionals (AITP), and Project Management Institute (PMI) chapters in the Richmond, VA area. Carolyn also volunteers for the PMI's Educational Fund as a project management instructor for non-profit organizations.