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GMP in Cross-Border Pharma: Why Manufacturing Standards That Pass in Europe Don't Always Satisfy the SFDA
Good Manufacturing Practice is frequently described as a universal standard, the core principles globally harmonized through the International Council for Harmonisation (ICH) and the Pharmaceutical Inspection Co-operation Scheme (PIC/S).
3 min read
Inside the SFDA: How Saudi Arabia's Drug Regulator Evaluates Pharmaceutical Dossiers: And How to Prepare One That Succeeds
In a pharmaceutical market growing at 10% annually, where 70% of medications are still imported, the Saudi Food and Drug Authority (SFDA) is the most consequential regulatory gatekeeper in the MENA region.
4 min read
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