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    U.S. Import of FDA Regulated Products: Understanding the Entry Process

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    Website http://bit.ly/2ydukgj | Want to Edit it Edit Freely

    Category fda regulatory training, fda regulatory training courses

    Deadline: October 25, 2017 | Date: October 25, 2017

    Venue/Country: Colorado, U.S.A

    Updated: 2017-09-26 15:35:14 (GMT+9)

    Call For Papers - CFP

    OVERVIEW

    This trade webinar will explain the complex US entry process so companies that import FDA regulated products will benefit from a better understanding of how the process works. It will discuss factors and actions that can lead to an import shipment being delayed or not allowed entry into the USA.

    WHY SHOULD YOU ATTEND

    U.S. Importers of FDA regulated products must know and comply with FDA and Customs’ import requirements. They are expected to use reasonable care when making entry on their merchandise and be prepared to demonstrate compliance with U.S. health and safety standards.

    Attend this webinar if you are importer of FDA regulated products or sell regulated products to U.S. importers and wish to have a better understanding of how FDA regulated products are entered into the U.S. Those new to importing FDA regulated products will also benefit from this webinar because we will explain some of the key terms, concepts and issues U.S. importers of FDA regulated products are likely to encounter. We will discuss the Customs entry process, Customs bond requirements for regulated products; HTS classification of regulated products; FDA import product codes; FDA affirmation of compliance numbers and the FDA entry.

    Attending this FDA regulatory training will help you to better manage your import compliance activities and help support your logistics supply chain.

    AREAS COVERED

    • Customs entry process

    • Customs bond requirements

    • Common U.S. Import documentation

    • Common U.S. trade terms and definitions

    • HTS classification of regulated products

    • FDA import product codes

    • FDA import affirmation of compliance codes

    • FDA Prior Notice

    • FDA ITACS system

    • FDA entry review process

    WHO WILL BENEFIT

    • U.S. importers of FDA regulated products

    • New U.S. importers of FDA regulated products

    • Foreign exporters of FDA regulated products (companies which sell regulated products to U.S. importers)

    • Purchasing department personnel for U.S. importers of FDA regulated products

    • Compliance officers

    • Logistics/Supply chain managers and analysts

    • Trade regulatory/legislative affairs professionals

    • Sales/marketing personnel

    • Training personnel

    • Consultants

    • International business operations

    • Chief Executive Officers

    • Customs or Trade Compliance Personnel or Officers

    • Import or Global Trade Directors or Managers

    • Import Supervisors

    LEARNING OBJECTIVES

    • How to manage the entry process to ensure import compliance and timely release of merchandise.

    • Tips on classifying FDA regulated products

    • How to find an FDA import product code

    For more detail please click on this below link:

    http://bit.ly/2ydukgj

    Email: supportattrainingdoyens.com

    Toll Free: +1-888-300-8494

    Tel: +1-720-996-1616

    Fax: +1-888-909-1882


    Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
    Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.