Clinical Trial Design

Research Services

We help you build robust, scientifically sound, and predictable clinical trials.

Why choose our partner network?

Designing a clinical trial can be a complex and daunting task. Our qualified partners help you boost the predictability and resource-efficiency of your study from the very start. From feasibility research to site selection, protocol development, and the drafting of a robust clinical development plan, we offer a holistic approach that ensures you are primed for success.

Our approach to clinical trial design

With a proven track-record in various therapeutic areas, we are committed to help you boost the innovation potential, scientific integrity, and real-world impact of your clinical study. We leverage our strong background in the design and management of complex studies to turn your vision into reality.

Triall has built a network of selected CRO partners who each excel in their respective domain, allowing us to offer you a truly end-to-end service offering. Each partner has undergone a rigorous vendor qualification to ensure our services meet the highest standards.

Feasibility Research

We conduct a thorough feasibility assessment to identify the optimal path for your clinical trial. Leveraging our vast network and deep industry insights, we analyse a multitude of factors including patient demographics, regulatory landscapes, and competitor studies. This data-driven approach allows us to provide you with a clear understanding of potential challenges and opportunities, enabling informed decision-making in study planning and design.

Site Selection

Choosing the right sites for your clinical trial is crucial for ensuring efficient patient recruitment, data integrity, and regulatory compliance. Our strategic site selection services consider a range of factors, including geographic location, site reputation, patient population, and local regulations to determine the most appropriate study sites.

Protocol Development

We work closely with your team to develop a precise, ethically sound, and comprehensive study protocol that serves as the blueprint for your clinical trial's success. The result is a protocol that is not only robust and compliant with regulatory requirements, but also fully aligned with your specific study objectives and requirements.

Endpoint Selection

We help you determine the most suitable primary and secondary endpoints that align with your study objectives and clinical questions. Our team ensures chosen endpoints are reliable, measurable, and responsive, which is integral for assessing the efficacy of a treatment. Through our service, you'll have endpoints that are both scientifically sound and meaningful to your research.

Clinical Development Plan

Crafting a comprehensive clinical development plan requires foresight, strategy, and meticulous planning. Our team of seasoned professionals collaborates closely with you to develop a tailored roadmap that outlines key milestones, timelines, and potential risks from pre-clinical research to late-stage clinical trials and regulatory approval. We consider scientific rationale, regulatory compliance, and the competitive landscape to create a plan that maximizes efficiency and minimizes uncertainty throughout the entire clinical development journey.

Tailored Precision

We recognise that every clinical trial  is unique. Our team of seasoned experts works closely with you to craft a  study design that aligns with your specific study objectives, patient  population, and therapeutic area.

Data-Driven Decisions

Our approach is grounded in data and insights, empowering you to make  proactive and informed decisions across study planning and design activities.

Scientific Excellence

With a deep-rooted commitment to scientific excellence, we integrate the  latest advancements in clinical research methodology into your study design.  Our meticulous approach maximises the potential for successful outcomes.

Strategic Vision

Next to scientific excellence, we enable strategic foresight. We help you  navigate the complex landscape of clinical development, anticipating  challenges and seizing opportunities along the way, ultimately optimising the  path towards regulatory approval.

Optimal Efficiency

By implementing cutting-edge methodologies and innovative trial designs,  we optimise the efficiency of your study, reducing timelines and costs while  maintaining scientific rigor.

Interested in this service?

Our specialists are available to answer your questions. Reach out to us and explore opportunities to match your clinical research needs today.

Did you know we also offer eClinical solutions?