FDA Regulation of Dietary Supplement Imports into the US
Date: December 24, 2024
Duration: 60 Minutes
Time: 12 PM EST
In 2010, FDA published the final rule governing importing of all dietary supplements into the US. This rule consolidated the previous rules for GMP, documentation, packaging and labeling, ingredient testing, and adverse event reporting requirements. The rules describe in great details the import and marketing requirements for all dietary supplements prior to import into the country or getting into US market, if manufactured domestically. Additional requirements such as Foreign Supplier Verification Program (FSVP) and third-party audit program have been proposed to further regulate the import of dietary supplements into the US.
This seminar will provide practical instructions to meet the current requirements in the process of manufacture and import of dietary supplements including description of key terms, concepts, and common issues that dietary supplement manufacturers are likely to encounter.
This seminar is intended for manufacturers and importers of dietary supplements who wish to have a better understanding of how FDA regulates dietary supplements and the custom clearance requirements for such products. Attendees will be introduced to the various rules that apply to dietary supplements and how to navigate the Customs entry process. Attending this training will help you to better manage your import compliance activities and help support your logistics supply chain.
Areas Covered in the Session:
- Current rules of dietary supplement new ingredients
- Documentation and labeling requirements
- Facility registration for manufacturing sites
- Import and domestic field exams
- Import investigations and sampling
- Role of US import agent
- Dealing with refusal to entry or delay in entry hold
Who will benefit:
The following individuals or disciplines will benefit from attending this Webinar:
- U.S. importers of dietary supplements
- Foreign exporters of dietary supplements
- Compliance officers
- Logistics/Supply chain managers and analysts
- Trade regulatory/legislative affairs professionals
- Sales/marketing personnel
- International business operations
- Customs or Trade Compliance Personnel or Officers
- Import or Global Trade Directors or Managers
- Import Supervisors
- Customs Brokers
Speaker: Mukesh Kumar
PhD, RAC | CEO, FDAMap
For more info, fill the box below. We will contact you within 24 hrs.
Webinar Fee
Prices are in US Dollars.
The registration fee includes: The live webinar & all related course materials.
Terms & Conditions to register for the Webinar
Your Registration for the workshop is subject to following terms and conditions. If you need any clarification before registering for this webinar please email us at info@fdamap.com
Payment
We accept credit card, debit card, and PayPal.
Cancellations & Substitutions:
Written cancellations through fax or email (from the person who has registered for this conference) received at least 5 business days prior to the start date of the event will receive a refund — less a $30 administration fee. No cancellations will be accepted — nor refunds issued — within 5 business days before the start date of the event. You may however, choose to substitute the webinar for which you are registered with some other webinar in the future.
On request by email or fax (before the seminar) a credit for the amount paid minus administration fees ($30) will be transferred to any future FDA Map event and a credit note will be issued. No-shows will be charged the full amount.
Webinar material will be uploaded on the website 24 hours before the scheduled date of the webinar. In case it is not available on the website due to some technical issues, we will email the material a few hours before the start of the webinar.
In the event FDA Map cancels the webinar, FDA Map will issue a full refund to all the registrants for that webinar. Some topics and speakers may be subject to change without notice.
