Dr. Mohamad Toutounji

Dr. Mohamad Toutounji (Germany) Dr. Mohamad Toutounji is a specialized consultant in CMC and GMP Compliance, with more than ten years of hands-on experience leading pharmaceutical development projects from early laboratory research to full-scale commercial manufacturing.

Dr. Toutounji supports pharmaceutical companies, emerging biotech firms, and contract development and manufacturing organizations (CDMOs) by designing integrated strategies that ensure product quality and regulatory compliance. His technical and scientific expertise spans a wide range of advanced therapeutic platforms, including:
• Cell & Gene Therapy
• mRNA-based therapies and modern genetic technologies
• Small Molecule development
• Antibody–Drug Conjugates (ADCs)

Throughout his career, Dr. Toutounji has played a key role in:
• Optimizing industrial processes and addressing development gaps
• Leading technology transfer activities across research, clinical, and manufacturing stages
• Building and enhancing quality systems and operational controls aligned with GMP standards
• Preparing regulatory submissions such as IND and IMPD, while guiding development teams toward complete compliance

Dr. Toutounji combines deep scientific knowledge in molecular biology and manufacturing technologies with practical experience in the pharmaceutical and MedTech industries, enabling him to deliver actionable and scalable solutions tailored to real-world production environments.

He also contributes to capability-building within scientific and operational teams through specialized training and strategic consulting. His work supports the development of modern, regulation-aligned pharmaceutical infrastructures—particularly in regions working to advance their healthcare and manufacturing capabilities, such as Syria