E&B Pharm Concilium supports pharmaceutical companies in accelerating their projects, from API development through regulatory submission, across all stages of the development lifecycle.
Consultant development chemical pharmaceutical regulatory
Moving beyond standard approaches to design solutions that are simpler, faster and more effective.
About E&B Pharm Concilium
E&B Pharm Concilium brings together two senior executives from the pharmaceutical industry with more than 40 years of combined experience and highly complementary expertise. Emilie, an expert in regulatory affairs, clinical development and marketing authorisation strategy, and Babak, a specialist in chemical and process development from API to finished product, provide a complete and integrated understanding of drug development.
We work alongside R&D, regulatory affairs and executive teams to propose secure development pathways, accelerate decision‑making and maximise project value, from the initial design through to market access.
Our signature combines scientific excellence, regulatory insight and pragmatic decision‑making to turn complexity into a sustainable strategic advantage for our clients.
Babak SAYAH
Emilie HUYGHUES des ETAGES
40+
Years of combined expertise
30+
Marketing authorizations and CE marks obtained
20+
Pharmaceutical development projects
Agencies
US-FDA, EMA, PMDA, ANSM, BfArM, ANVISA, TGA
Our Values & Commitment
At E&B Pharm Concilium, our approach is built on core principles that ensure the excellence of our advice and the success of your pharmaceutical development projects.
Integrity
An unwavering commitment to ethics and transparency, ensuring reliability and compliance at every stage of your regulatory projects.
Rigor
Flawless scientific and regulatory rigor to secure your submissions and development strategies.
Ingenuity
Designing agile and innovative solutions to overcome complex development challenges and accelerates your product's market access.
Our commitment:
Turning technical and regulatory complexity into a competitive advantage
From API to finished product, we support the development and optimisation of your processes.
Services
Designing a program is one thing ... getting the Regulatory Authorities to buy in is another!
We lead your pharmaceutical development programs by integrating all CMC, quality, non‑clinical and clinical aspects.
We design pragmatic and innovative regulatory strategies for your marketing authorisation dossiers and territorial extensions.
We perform critical reviews of CMC, development and regulatory data to inform your acquisition or partnership decisions.