Pharmaceutical & Biotech Companies

Organizations developing therapies for genetic disorders looking for patient-journey insights, treatment barriers, and community engagement pathways.

Contract Research Organizations (CROs)

Research networks collaborating on trial readiness, patient navigation, and ethical recruitment in high-burden populations.

IRBs & Ethics Committees

Partners needing culturally informed guidance, consent pathway support, and clarity on cross-border participant understanding.

Research Institutes & Universities

Academic partners studying hematology, global health, gene therapy, and treatment innovation requiring real-world case data.

Health Data & Innovation Companies

Digital health, AI, and data-analytics companies leveraging sickle-cell insights, experience mapping, and early treatment trends.

Corporate Social Responsibility (CSR)

Companies seeking to support sickle-cell communities through access programs, sponsorships, patient education, and global health initiatives.