This whitepaper examines how adaptive clinical trial designs in oncology can improve patient outcomes and treatment efficacy through real-time modifications, while also highlighting the regulatory and ethical challenges these designs pose within IRB frameworks. 

Overcome gene synthesis roadblocks. Discover how enzymatic DNA synthesis enables production of complex, high-GC, and regulatory sequences—unlocking progress where traditional methods fall short. Download now!

We interviewed 24 Medical Affairs leaders on the critical success factors for building a Best Practice Medical Affairs organization. This report shares what we learned.

Learn how subcutaneous delivery helps drug developers stand out, improve patient experience, and drive growth. This white paper covers key drivers, common myths, and real-world success stories. Download now to see how on-body devices simplify the switch.