Biomapas Insights: Selecting the Right CRO at the right time – What Biotechs Need to Know

Expert insights on timing, selection criteria, and early-phase clinical trial strategy for choosing the right CRO in biotech development.
In this episode, Indrė Dryžienė, Head of Clinical Operations Project Management at Biomapas, is joined by Samson Fung, Managing Director of Fung Consulting Healthcare & Life Sciences, and Artūras Pažera, Senior Clinical Project Manager at Biomapas, to discuss key questions on how CRO selection shapes early-phase biotech success.

Choosing a CRO directly influences speed, feasibility, regulatory clarity, and study quality. Hence, for emerging biotechs planning early-phase and first-in-human studies, the right timing and partnership can prevent delays, strengthen operational efficiency, and improve decision-making from the very start.

During the discussion, we explore:

  • The most common mistakes biotechs make when planning their first trial
  • When sponsors should start thinking about their CRO partner
  • What matters most when evaluating a CRO for early-phase studies
  • How do smaller CROs compare to global providers in early oncology development
  • How early regulatory or scientific advice can change the trajectory of a study

Whether you are preparing for your first-in-human study or scaling early-phase oncology programs, this conversation offers grounded, experience-driven guidance.

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...

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