In August 2024, RADEX experts welcomed the dedicated ZAKKO Group Nasma team from Iraq to Jordan for an intensive, tailor-made program. The training focused on crucial regulatory areas, including:
GMP and Manufacturing Site Accreditation: Covering compliance for the USA, Europe, Jordan, and Saudi Arabia.
Biologics and Biosimilars: In-depth regulations and regulatory submissions specific to the USA and Europe.
Medical Devices Regulations and Regulatory Submissions: With a focus on Europe (MDR) and Jordan.
This bespoke training was designed to provide the Nasma team with highly specialized, practical knowledge directly applicable to their operations. It was a truly enriching experience, fostering advanced expertise and strengthening their capabilities in complex global regulatory landscapes.
RADEX is proud to support leading pharmaceutical companies like ZAKKO Group in their pursuit of regulatory excellence!