Biomapas Insights: Clinical Site Selection for Early Phase Oncology Studies

Expert perspectives on where to begin, how to choose the right clinical sites, and what to consider when selecting an eCRF/EDC system for early-phase oncology studies.
In this episode, Artūras Pažera, Senior Clinical Project Manager at Biomapas, speaks with Jean‑Luc Béjot, an independent consultant with more than 35 years of international experience in clinical development, clinical operations, and medical affairs.

Together, they explore essential considerations that shape the success of first‑in‑human and early-phase oncology trials:

  • Where small biotechs should begin when planning an early-phase oncology trial.
  • How to identify the right clinical sites and balance expertise with recruitment potential.
  • What to look for when choosing an eCRF/EDC system for small, adaptive early‑phase studies.

Whether you are preparing your first early-phase trial or optimising ongoing oncology programs, this episode provides experience‑driven insights to help sponsors plan smarter and execute with confidence.

Choosing the Right QPPV Partner for EU and Global Compliance

Choosing the Right QPPV Partner for EU and Global Compliance

Pharmacovigilance outsourcing has become crucial for biotech companies to remain compliant and safeguard patients. When you bring a drug to market in Europe or globally, your Qualified Person for Pharmacovigilance (QPPV) serves as your first line of defense. The right...

Big Enough To Cover  All Your Needs. Small Enough To Care.

Discover the tailored solutions that Biomapas provides to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Regulatory Affairs

Pharmacovigilance

Medical Information

Big Enough To Cover All Your Needs.
Small Enough To Care.

Discover how Biomapas provides all the support to accelerate your clinical trials and optimize your drug development process.

Clinical Research

Reliable support for every phase of your clinical trial, from recruitment to results.

Pharmacovigilance

Flexible safety monitoring to keep your products compliant and trusted.

Regulatory Affairs

Confidently navigate regulatory challenges with expert support.

Medical Information

Clear, accurate medical information 24/7, tailored for global audiences.

Quality Assurance

Export auditors help identify gaps and close them with actionable solutions.