About us

Background

DELPHINIUM is a dedicated and dynamic company, comprised of experienced professionals committed to Phase I clinical trials. Our 12-bed Phase I clinic specializes in clinical studies conducted with healthy volunteers, offering a range of services including Project Management, Monitoring, Data Management, Bioanalysis and more.

Our mission is to deliver high-quality, tailor-made Phase I clinical studies in which we prioritize efficient and direct communication between Sponsors and researchers to ensure a flexible, fast and adaptive approach to your clinical program. At DELPHINIUM, we are committed to excellence and precision in every aspect, ensuring the success of your clinical trials.

Challenges

We recognize the unique challenges faced by biotech companies in executing Phase I programs with tight timelines and limited budgets. Partner with DELPHINIUM to collaborate with a CRO that is fully committed to addressing your challenges and helping you achieve your clinical trial goals.

We believe that the combination of experience, dedication, and a personalized approach leads to the highest quality outcomes, even when unforeseen events arise. Together, we can advance the frontiers of medical science.

How DELPHINIUM supports you

We offer tailored support for organizations involved in early-phase research, including healthcare providers, life sciences companies, and academic environments. Our core services include:

Team training in clinical research
DELPHINIUM helps build internal expertise through our Clinical Research Nurse Academy by covering ethics submission, protocol interpretation, essential documents, consent procedures, and more. Visit our Clinical Research Nurse Academy page for details.
Skilled support staff
Whether you need a short-term boost or long-term cover, we can provide experienced Research Coordinators (CRCs) who skillfully manage patient visits, data entry, and communication with investigators.
Audit and inspection readiness
If your team has some experience but lacks the specific expertise to achieve audit and inspection readiness, DELPHINIUM is here to help. From data validation and query resolution to ensuring a complete and compliant Investigator Site File, we provide the knowledge and tools your team needs to confidently prepare for inspections.
Regulatory support
Our regulatory specialists assist with IRB/REC submissions, amendments, and response management, ensuring your filings are compliant and timely.
Trial start-up consulting
Planning your first early-phase trial? Our consultants guide you through feasibility assessment, site selection, trial logistics, and study setup.

Why choose DELPHINIUM

At DELPHINIUM, we offer flexibility to match your needs, whether you require short-term support or a long-term partnership, we adapt accordingly. Our team brings deep, hands-on expertise in early-phase research, ensuring your projects are guided by experienced professionals. Compliance is at the core of everything we do; we operate in alignment with ICH-GCP standards and local regulatory requirements to maintain the highest level of quality and integrity.

Our management

Christine Voors-Pette, MD has been working as a Principal Investigator for over 15 years in both early- and late phase clinical research. She performed over 50 early phase clinical studies, with the majority being First-in-human trials. She is known for her straight forward approach, open communication and her commitment to clients, volunteers and coworkers.

Jitske Beukema brings a wealth of knowledge and experience within pharmaceutical and Biotech industry. She is an accomplished and proven senior executive with more than 30 years of experience in Phase I healthy volunteer and patient studies.

Agnes Boelens-van Nieff has been working for 20 years as Management Assistant/Sr. Clinical Trial Assistant/Regulatory Affairs Specialist. She will be responsible for regulatory affairs and financial affairs.