Founder & Principal

Haydar Celik, PhD, is a regulatory affairs executive with experience spanning biopharma, molecular diagnostics, regulatory consulting and translational research. His work focuses on the intersection of drug development and diagnostics, with particular expertise in precision medicine, biomarker strategy, IVD and companion diagnostic development, digital health, and AI/ML-enabled technologies.
Across FDA and industry roles, he has led and advised global regulatory strategies, health-authority interactions, evidence-generation plans and cross-functional programs supporting biomarker-driven drug and diagnostic development. His perspective combines regulatory science with a scientific background in oncology, translational research and molecular diagnostics.
Haydar has also advised executive teams, boards and investors on regulatory risk, product strategy and emerging technologies, and has contributed to industry collaborations and standards advancing molecular diagnostics and precision medicine.
Advancing Precision Medicine Through Strategic Leadership
Haydar Celik, PhD, is the Founder and Principal of the firm, leading with a vision to advance precision medicine through strategic innovation and regulatory excellence. With extensive experience at the FDA and broad exposure to global regulatory frameworks across the diagnostics and pharmaceutical industries, Haydar guides companies and investors through regulatory pathways and aligns innovation with strategic growth.
Focused on the intersection of diagnostics and drug development, he partners with life-science leaders to bring transformative diagnostic, digital-health, and personalized-medicine solutions to market.
Bridging Science, Regulation & Business
A recognized expert in precision medicine, diagnostics, biomarkers, and AI-driven health technologies, Haydar bridges science, regulation, and business to help organizations build sustainable leadership in an evolving healthcare landscape.
His work spans the full innovation ecosystem, from early product strategy and regulatory positioning to evidence generation and market access, advising executive teams and boards in making confident, high-impact decisions.
A Collaborative Approach to Innovation
Known for his collaborative leadership and clear strategic perspective, Haydar champions innovation that is both visionary and grounded in real-world value.
His global outlook and dedication to advancing personalized healthcare continue to shape the future of diagnostics and life-science innovation.
Beyond the Office
Outside work, Haydar enjoys traveling, gardening, spending time outdoors with his family, and exploring philosophy and the intersection between science and human experience.
Turn complex scientific and regulatory challenges into clear, actionable strategies. Blue Tulip Solutions helps life-science organizations reduce risk, strengthen product positioning, and accelerate the path from innovation to market. Our integrated approach connects science, regulation, and business to support confident decisions and sustainable growth.

Navigate FDA and global regulatory pathways with clarity and confidence.

Advance biomarker-driven development and personalized healthcare through integrated strategy.

Bridge scientific discovery with market adoption, access, and long-term product value.

Support executive teams and boards in making informed, high-impact strategic decisions.

Support executive teams and boards in making informed, high impact strategic decisions.

Bridge scientific discovery with market adoption, access, and long-term product value.
Contact Blue Tulip to discuss your needs and discover how we can help you thrive.

Expert Consulting from Concept to Commercialization in Precision Medicine
(301) 919-8573
(301) 919-8573
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