We offer full support for sample size calculations, protocol design, randomisation, analysis, and reporting.
In the complex world of clinical trials, the integral role of biostatistics cannot be overstated. Utilising best practice methodologies and years of expertise, our qualified biostatistics partners help you navigate the complexities of data interpretation and elevate the scientific rigour of your study results.
Engage with our seasoned team of biostatistics experts who can provide tailored support to fit the unique needs of your study. Together we can transform your raw study data into meaningful insights that drive regulatory approval and accelerate your road-to-market.
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.
Collaborate with our biostatisticians right from the start to design studies that are statistically sound, efficient, and aligned with your research objectives. We'll help you choose the right sample size, randomisation techniques, and endpoints to maximise the value of your trial.
Our team of experts review your study protocol to ensure its alignment with the latest biostatistical methodologies and study design principles. We help you create a robust protocol that adheres to regulatory standards and optimises the statistical integrity of your trial.
We help you create a detailed Statistical Analysis Plan (SAP), defining the precise statistical methods for analysis, as per your study objectives. Our SAPs are designed to ensure completeness, appropriateness, and compliance with regulatory guidelines.
Randomisation is a critical aspect of unbiased clinical research. Our biostatisticians devise robust randomisation procedures to reduce bias and ensure validity. We carry out the unblinding process carefully, maintaining adhering to protocol and data integrity principles.
We leverage the latest software for precise data analysis and digital data review. Moreover, our robust reporting system allows for clear interpretation and consistent, accurate results. This empowers our team to provide you with the statistical reports required for your regulatory submissions.
Our seasoned biostatisticians bring a wealth of experience across diverse therapeutic areas, enabling us to tailor our services to your specific study needs and requirements.
We go beyond the numbers – our team translates statistical findings into actionable recommendations, enabling you to make well-informed decisions that increase the changes of clinical trial success.
We understand the critical role of compliance in clinical research. Our services align with quality standards and regulatory requirements, ensuring the integrity and validity of your study data.
We believe in partnership. Our biostatisticians seamlessly integrate with your team by means of clear communication and expert guidance throughout the clinical trial lifecycle. This approach ensures that your study’s statistical components seamlessly integrate with your core study objectives.
Our specialists are available to answer your questions. Reach out to us and explore opportunities to match your clinical research needs today.
