Helping you navigate complex challenges with confidence.
 

I’m a regulatory affairs consultant with a global perspective and a strong scientific foundation. I specialize in biologics, with a particular focus on cell and gene therapies, and I work closely with companies to support the development and approval of innovative therapies.
 

With experience spanning clinical trial applications, agency interactions, and life-cycle management, I have led regulatory teams and engaged with key health authorities like the EMA and FDA. I understand the complexities of this rapidly evolving field, and how to move through them strategically and efficiently.
 

I hold a PhD in Biochemistry and a Master’s in Drug Regulatory Affairs, which allows me to combine scientific insight with regulatory know-how. Whether you are advancing a new therapy, entering new markets, or looking for hands-on support, I’ll help you anticipate challenges, stay compliant, and keep development moving forward.
 

Let’s work together to bring your innovation closer to the patients who need it!