NAMA Bio-Center
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Training & Capacity Building

GCP, bioequivalence and regulatory training for sponsors, CROs and investigators.

The NAMA Bio-Center training room from the back of the seating, with rows of black chairs and side writing tables facing two wall-mounted screens on the wood-panelled front wall.

What this covers

NAMA Bio-Center runs structured training programs for pharmaceutical companies, CROs, investigators, and clinical research staff, delivered in the center’s own training and meeting rooms.

  1. Good Clinical Practice (GCP) training

    Comprehensive programs aligned with ICH-GCP guidelines, ensuring ethical conduct, subject protection, and data integrity in clinical research.

  2. Bioequivalence training

    Specialized training covering bioequivalence study concepts, protocol execution, sample handling, and clinical trial operations.

  3. Regulatory & quality training

    Practical sessions on SFDA requirements, SOP implementation, quality management systems, and audit preparedness.

  4. Customized institutional training

    Tailored programs developed for pharmaceutical companies, CROs, investigators, and clinical research staff based on operational needs.

Trained people are infrastructure too. Every programme we run adds capacity the Saudi research ecosystem keeps.

Ready to run your BE programme in the Kingdom?

Tell us the molecule, the dosage form and the timeline you are working to. We will come back with a study design and a schedule.

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