Peri & Post Approval Services

From Real World Research to Observational Studies

Peri & Post Approval Services

From Real World Research to Observational Studies

Real-World Research for Real-World Outcome
Exom combines multi-disciplinary expertise, and integrated technologies to help you to produce the real-world evidence you need to build your brand value and establish a strong market position,  while maintaining regulatory compliance.

Late phase clinical trials
Our dedicated late-phase CRO services include “full service” support for interventional Phase IIIb and Phase IV studies, peri and post-marketing observational studies, pragmatic trials, post-authorization safety studies (PASS), post-authorization efficacy studies (PAES) to evaluate  effectiveness and safety in a real-world setting.

Observational studies
Observational studies provide valuable insights into the causal association between a treatment (e.g. a drug product, device, or procedure) and a particular event or outcome (e.g. long-term effectiveness and safety).
The non-interventional studies have become critical tools in health care research because they offer a broader range of approaches to answering important, “real world” clinical research and product usage questions.

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Exom is now Kapadi

 

Once three entities – OncoBay Clinical, Clinscience, and Exom Group s.r.l – now we stand as one, bringing forth a symphony of expertise and seamless operations. To celebrate our unity, we re-brand under the banner of Kapadi, and embark on a new chapter of exceptional service in oncology clinical research.

Kapadi is not just a name; it's a testament to our fusion. It signifies the our standing as a global CRO powerhouse committed to accelerating groundbreaking cancer therapies that uplift patients worldwide. From conceptualizing studies, navigating regulations, and analyzing data, we provide a comprehensive array of services designed to empower your oncology clinical trials.

Visit Kapadi.com