Clinical Research News

See how CRO safety writing support helped a global pharmaceutical company prepare a signal evaluation report, with clear benefit-risk assessment for a health authority response under tight timelines.

Explore global regulatory frameworks and ISO 18562 standards guiding toxicological risk assessment for safe medical devices.

Case study on how an aligned biometrics partnership supports smoother clinical data management, reusable standards and continuity across studies.

Read how our longstanding partnership with Chiesi Farmaceutici supports complex clinical pharmacology and first-in-human trials with expertise, reliability and efficiency.

Explore how our leading medical writing services CRO supported complex clinical trial protocol development and regulatory alignment across global Health  Authorities in a high-risk indication.

Expert insights into how operational pressure affects IDMC performance in clinical trials and what enables structured discussions, alignment and efficient decision-making.

Expert insights into recurring challenges in IDMC execution across clinical trials, showing how data, timing and setup affect the efficiency, cost and flow of decision-making.

How we adapt clinical research to biotech and pharma needs in Europe, with CHIM, ADME, biometrics and data innovation for faster insights.

Learn why so few Respiratory Syncytial Virus (RSV) models exist, what makes them so complex and how Antwerp emerged as a leading European hub for human challenge research.

Explore how Antwerp’s validated challenge models, GMP capabilities and clinical expertise create a true early phase advantage as Belgium extends accelerated timelines to CHIM trials, with approvals capped at 59 days.