Wilding Statistical Consulting

We offer expert statistical consulting services to pharmaceutical and biotechnology companies, academic institutions, government organizations, and projects spanning health, biology, environmental, and social sciences. Our team of experienced professionals is dedicated to helping you make data-driven decisions that propel your projects forward. We offer personalized service, direct communication with our experts, flexibility, and cost-effectiveness, ensuring you receive the best value for your investment. We offer a comprehensive range of services to meet your statistical needs: • Study design: Expert guidance in designing clinical trials (e.g., Phase I-III therapeutic trials, medical device trials), epidemiological studies (case-control, cross-sectional, and cohort), and other studies, considering feasibility constraints. • Hypothesis formulation: Collaborating with investigators to define hypotheses and refine study questions. • Sample-size and power calculations to ensure robust study design. • Protocol development: Reviewing, creating, and refining study protocols as needed. • Randomization plan design and implementation for unbiased study outcomes. • Creation of Statistical Analysis Plans (SAPs), adhering to ICH/FDA guidelines when appropriate. • Statistical study oversight and monitoring for quality assurance. • Statistical analyses and reporting: Conducting statistical analyses, interpreting study findings, and contributing to the final study report. • Preparation of abstracts and manuscripts for publication, showcasing your research findings. • Assisting with regulatory submissions to meet requirements.