Medical Foods: Practical Tips to Meet Latest FDA Requirements for Claims and Quality

Date: April 22, 2024
Duration: 60 Minutes
Time: 12 PM EST

​Medical foods play an important role in the management of patients with special dietary restrictions and needs. The designation of medical food by FDA implies special handling, labeling, distribution and manufacturing requirements. The manufacturing requirements for such products can be complex and manufacturers are often worried about effective compliance for medical foods. This webinar will discuss the regulatory processes to designate and market a product as medical food. Common issues with FDA compliance and the potential solutions will be discussed using case studies. 
 

Why should you attend:

Medical foods designation comes with its own set of regulatory responsibilities. FDA expects manufacturers to self-assure compliance status and reserves the option to audit all aspects of the manufacturing, labeling and distribution as it deems necessary. This webinar fills the gap in knowledge in terms of the FDA expectations from medical foods and way to address common deficiencies. The case studies discussed will further highlight potential audit issues, training requirements, good manufacturing practices for medical foods, and marketing issues.  

Areas Covered in the Session:

  • Current FDA accepted definition of medical foods and functions foods
  • Medical foods and dietary supplements
  • Good manufacturing practices for medical foods
  • Best practices for marketing and distribution
  • Review of case-studies from unsuccessful and successful marketing of medical foods
  • Practical tips for training of sales and marketing teams in medical foods
  • Regulatory strategies for designating dietary supplements and medical foods  

Who will benefit:

This webinar will provide valuable information to:

  • Manufacturers of medical foods
  • Physicians and hospital personnel
  • Dietary supplement manufacturers
  • Marketing and advertising professionals
  • Regulatory affairs professionals, research analysts

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.

For any information on the training agenda and logistics, please call +1 410-501-5777 or email: info@fdamap.com