We act as the Virtual Preclinical Department for MENA biotechs. We de-risk drug development, ensure SFDA/ICH compliance, and train clinical teams to leverage AI.
Regulatory Insider Expertise
Clinical Trial Optimization
World-Class Pharmacology Pedigree
From early-stage pharmacological validation to clinical AI deployment, we provide bespoke intelligence and strategic auditing.
We perform rigorous gap analysis and study design auditing against SFDA, ICH, and ISO guidelines to prevent costly IND/CTA rejections before they happen.
We upskill clinical teams, deploying specialized training modules to help pharmaceutical organizations safely integrate AI and LLMs into trial design and regulatory workflows.
Bespoke scientific advisory focusing on complex GPCR signaling, target safety, and mechanisms of action to bridge the gap between discovery and clinical viability.
Founder & Principal Consultant (PharmB, MSc, PhD, FHEA)
Dr. Safar provides Roaa Biomedical with an unparalleled dual-vantage point: the Innovator and the Regulator.
Whether you need an SFDA compliance audit, advanced pharmacological strategy, or AI integration training for your clinical team, we are ready to partner with you.
Reach out to us directly to initiate a conversation:
m.safar@roaa.co.uk