On-Demand Webinar - Saudi Arabia 2019: Building Your Comprehensive Compliance Strategy

June 27, 2019

In early 2019, the Saudi Food and Drug Authority (SFDA) initiated reporting requirements that affect all companies producing medicines for the Saudi Arabia market. Manufacturers need to understand how they can comply immediately with SFDA regulations—and prepare for aggregation in October 2019. How do they register with SFDA? What operations will need to be reported to the Saudi track-and-trace system? How will trade partners exchange information as products move through the Saudi supply chain?

In this on-demand webinar, Solutions Consultant Ayman Waneis and Industry Marketing Director Allan Bowyer provide a detailed overview of the business and operational challenges companies face in the Saudi Arabia market—and how TraceLink supports a comprehensive approach to SFDA compliance.

You will learn about:

Saudi Arabia requirements
Planning for Saudi Arabia aggregation
Challenges in post-manufacturing serialization
TraceLink Saudi Arabia solution platform

Aggregation, Basics, Pharmaceutical, Saudi Arabia

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Saudi Aggregation 2019: Potential Impact and 3 Steps You Can Take Today

See what you can do to prepare for the October 2019 aggregation requirement.

Saudi Arabia: Understanding the Compliance Requirements

See key Saudi deadlines, roles and responsibilities, packaging elements, and more.

Saudi Regulations are in Force: How Are You Complying?

Learn more about your options for meeting current and future Saudi compliance requirements.

Saudi Arabia and Egypt: Regulatory Update

Brian Daleiden, TraceLink VP of Industry Marketing, provides a 5 minute update on 2018 developments.

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