Principle Standing Committee and Subcommittees:
The Transportation Committee (Chair Kim Calicott/Vice Chair Rich Roche)
includes the following Subcommittees:
- Air Freight Subcommittee
- NVOCC Subcommittee
- Logistics Subcommittee
- Export |Compliance Subcommittee
The Customs Committee (Chair Sandy Langford-Coty/Vice Chair Ralph De La Rosa)
includes the following:
- ACE Strategy Subcommittee
- Part 111 Rewrite Subcommittee
- Trade Interruption and Resumption Planning Subcommittee
The Regulatory Agencies Committee (RAC) (Chair Mike Lahar/Vice Chair Adam Lees)
includes the following:
- USDA APHIS-Core Subcommittee
- USDA APHIS-Lacey Subcommittee
- USDA AMS-MO Subcommittee
- USDA AMS-Organic Subcommittee
- CPSC Subcommittee, EPA Subcommittee
- FCC Subcommittee, FDA Food Subcommittee
- FDA Devices-Tobacco Subcommittee
- FWS Subcommittee, NHTSA Subcommittee
- NOAA/NMFS Subcommittee
- TTB Subcommittee
- ATF Subcommittee, and DEA Subcommittee
Upcoming Meetings & Conferences
STR Webinar: Understanding U.S. Customs Origin Determinations in the Biopharma and Life Sciences Industry
Biopharma and life sciences companies face unique challenges when determining the country of origin for imports for research and development, clinical, and commercial cross-border transactions. These origin decisions must comply with U.S. customs laws for origin declaration for duty payments and origin marking, while also considering a myriad of other labeling concerns. This webinar provides an overview of basic U.S. customs law origin principles and highlights specific areas for review relevant to the industry.
Key Topics
Legal framework and importance of origin determination for the biopharma and life sciences industry
Substantial transformation for biopharma and life sciences
Small case studies of key U.S. Customs Rulings
Using origin as part of a duty reduction strategy
Risks with origin labeling and Partner Government Agencies
*Committee and BOD meetings are only open to Regular members