Regulatory Framework of Drugs in MENA: Insights

In this webinar, our experts discuss regulatory affairs of medicinal products. Two aspects that have recently gained increasing importance among the various stakeholders, namely the eCTD implementation across the region and the serialization and barcoding requirements for medicinal products.

So, we share our insights on these two aspects and share how you can avoid various issues in drug registration.

Planning your next product registration?

Let’s talk about how we can navigate eCTD and serialization to ensure smooth drug registration processes.
Global Literature Review: Ensuring Safety through Robust Processes

Global Literature Review: Ensuring Safety through Robust Processes

In pharmacovigilance, timely identification of safety signals is essential to protecting patients – which is why our Global Literature Review (GLR) process provides a systematic and reliable way to capture, analyze, and document safety data from trusted scientific...

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