Our data management and analysis services ensure the integrity and accuracy of clinical trial data. Using Electronic Data Capture (EDC) systems, we collect and store trial data securely while ensuring compliance and protocol adherence through clinical data monitoring. Our biostatistics team utilizes advanced statistical methods to evaluate trial outcomes, providing clear insights for decision-making. Additionally, we manage adverse events and safety reporting, ensuring that any potential risks are identified and mitigated, and implement Risk-Based Monitoring (RBM) to focus on high-risk sites for compliance.
Data Integrity & Reporting:
- Electronic Data Capture (EDC) Systems – Collecting, storing, and managing trial data.
- Clinical Data Monitoring – Ensuring data integrity, compliance, and protocol adherence.
- Biostatistics & Data Analysis – Evaluating trial outcomes using statistical methods.
- Adverse Event & Safety Reporting – Identifying, reporting, and mitigating adverse drug reactions (ADR).
- Risk-Based Monitoring (RBM) – Identifying high-risk sites and ensuring compliance.
Transform Your Vision into Reality
Contact Usahihi Therapeutics today to leverage our advanced services in clinical trials and therapeutic development. Start the conversation now and turn your idea into impact. Link to Contact Us page