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30 Weeks to EU FMD: Your Questions Answered
Watch this recording of a live webinar to hear Christoph Krähenbuhl answering audience questions on achieving EU FMD compliance.
Excellis Q&A: Why Phase 3 Manufacturers Shouldn’t Delay Serialization
See how Excellis Health Solutions avoids bottlenecks in serialization implementation, DSCSA challenges, and their philosophy behind phase 3 planning.
An Interview with Tjoapack: Innovation through Serialization
Learn how Tjoapack turned the challenge of updating packaging for EU FMD into an opportunity for innovation, in this on-demand webinar.
DSCSA Solution Questions from Pharmacy Legal & Compliance Teams
Pharmacy legal or compliance advisers must ensure compliance solutions meet the necessary DSCSA requirements. Read their FAQs.
Altran Q&A: Spain’s Small Pharmas Face Big Serialization Challenges for EU FMD
Understand the challenges small pharmas face as serialization approaches, and how industry expert Altran helps solve them.
ACS Q&A: Building a National System for EU FMD
Read an interview with ACS PharmaProtect to learn how the German national system works and how it will operate under EU FMD.
Laetus Q&A: How People, Process, and Planning Will Drive Your EU FMD Compliance Success
Track and Trace Manager at Laetus explains why humans have a major impact on traceability, and what insights supply chain companies can gain from…
Building for EU FMD - 5 Serialization Leaders Share How to Prepare
See how experts have overcome roadblocks as they implement Level 1-5 solutions for EU FMD serialization.
Validation and Automated Validation: Top Industry Questions
Get 27 answers covering the impact of validation to your requirements, resources, and risk—and how automation offloads the entire burden.
How Do I Prepare Product Master Data for EU FMD?
Learn what product master data you need to upload to the European Hub under EU FMD, and how to go about preparing it.