At ClinSite, we offer end-to-end management and handling of late phase clinical trial solutions and services for new investigational drugs and biologics across various therapeutic areas. With over a decade of experience, we are well-versed in the complexities of Phase II and Phase III clinical trials. We focus on achieving optimal outcomes with minimal time, effort and resources to ensure that the projects are completed smoothly and the highest global standards.

At ClinSite, we specialize in managing non-interventional studies, offering tailored Phase IV clinical trial solutions for evidence-based market management.    

Additionally, our registry studies provide in-depth insights by keeping detailed records of patient outcomes.

• Observational Studies
• Registry Studies
• Real World Evidence Studies
• Long Term Follow-up Studies

We work with our clients to assess the current situation in the clinical study and recommend the optimal pathway to possible clinical study rescue. Our services include:

• Feasibility of additional sites in existing locations
• Feasibility of addition of new countries and analysis of risks and benefits of expanding clinical trial geography
• Oversight and management of existing CRO vendor and review of existing project management practices for increased effectiveness

We offer comprehensive services for the development and clinical evaluation of medical devices and nutraceuticals. Our team provides end-to-end support, from regulatory consulting and clinical trial design to data management and post-market surveillance.