FDA Compliant Warehouse and Distribution Practices
Date: June 23, 2025
Duration: 60 Minutes
Time: 12 PM EST
Why you should attend?
This webinar will focus on all current regulations and FDA Guidance Documents related to supply chain management starting from acceptable practices for receipt of materials, control of intermediates, finished product storage and handling, release of materials, short-term and long-term storage, shipping practices, and recall management. Challenges and opportunities for FDA-compliance verification of warehousing and distribution will be discussed with examples from real world scenarios. Best practices for the control of flow and maintenance of goods will be discussed. This webinar will provide warehouse operators and third-party service providers alike, a measure to evaluate current practices for compliance with Good Storage/Warehouse Practices (GSP) and Good Distribution Practices (GDP) for drug and biotechnology products.
Areas Covered in the Session:
- Principles for Material Control in GMP Facilities
- Basic expectations from GSP and GDP
- Responsibility for Traceability and accountability
- Supply Chain Flow Charts
- Vendor validation for shipping and distribution
- Product recall management
Who will benefit:
- Personnel working in packaging, labeling, storage, and distribution
- Quality Control and Assurance
- Manufacturing and Packaging
- Managers, CEOs & Directors
- Warehouse Managers
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
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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.
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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.