Advancing Health Innovation

with Scientific Precision and Regulatory Expertise.

We support biotech, pharma, and medical device companies across the full development pathway, from preclinical research to market approval, with scientific rigor, regulatory certainty, and operational excellence.

Our DNA

Geistek Pharmaceuticals is a full-service Contract Research Organization (CRO) and Regulatory Affairs partner in the Life Sciences sector.

Founded in Spain and operating across Western Europe, Geistek brings together scientific rigor, operational excellence, and regulatory insight to accelerate the development of new therapies and medical technologies.

We combine the agility of a growing company with the quality standards of global CROs — partnering closely with our clients to transform innovation into approved, market-ready solutions.

Integrity & Ethics

Upholding the highest standards in every study and submission.

Scientific Rigor

Every project built on solid methodology and data.

Collaboration

Working side-by-side with sponsors and investigators.

Innovation

Using technology and expertise to optimize outcomes.

Our Geography

We operate across Western Europe:

At Geistek, we don’t just manage studies, we build partnerships.
Our integrated approach bridges science, regulation, and technology, helping you move faster with confidence and compliance.

Let’s accelerate your path from science to approval.

Whether you’re planning a first-in-human study, preparing a regulatory submission, or developing a medical device, our experts are here to help.