Full integrated CRO

for life sciences innovation

We support biotech, pharma, and medical device companies from preclinical research to regulatory approval.

About Us

Geistek is your trusted partner combining scientific rigor and regulatory expertise. Our 360° model guides companies from laboratory to market with confidence and compliance.

Use Cases

Services

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.

Regulatory Affairs

Global submissions, EMA/FDA pathways, compliance strategies.

Medical Writing

Clinical and regulatory documents: protocols, CSRs, CERs, dossiers.

Strategic Study Design

Tailored study design, endpoint strategy, feasibility & indication planning.

Clinical Trial Management

Full-service trial operations from Phase I–IV, site & patient management.

Data Management & Biostatistics

EDC setup, data cleaning, analysis, advanced statistics & AI models.

Why Choose Geistek

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.

Scientific Rigor with Regulatory Depth

We combine scientific expertise with a deep understanding of global regulations, ensuring every study and submission is designed to succeed the first time.

Full-Service, End-to-End Partner

From preclinical studies to regulatory approval and market access, we provide a 360° service that reduces complexity and accelerates development.

Flexible & Scalable Delivery

Whether you are a biotech start-up, a mid-size pharma, or a global device manufacturer, our models adapt to your needs, agile, cost-efficient, and always inspection-ready.

Strategic Partnership, Not Just Outsourcing

We act as an extension of your team, aligning with your goals, timelines, and compliance requirements, a true partner from science to approval.

Our Experience

At Geistek, we bring together proven expertise across biotech, pharma, and medical devices. Our track record demonstrates our ability to deliver complex projects with scientific rigor and regulatory precision.

When you partner with Geistek, you gain access to a global team that has seen, and solved, the challenges you face. From start-ups to global leaders, we help organizations bring safe, effective, and compliant therapies to patients worldwide.

Our Geography

We operate across Western Europe:

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.