Process Standardization and Documentation
Process standardization and documentation in a central lab ensure consistent sample handling, testing, and reporting, enhancing data reliability across all trial sites. Comprehensive documentation provides a clear audit trail, supports quality checks, and simplifies staff training by detailing each protocol step. This approach promotes regulatory compliance and strengthens the integrity of clinical trial outcomes.
Central Lab Manual Compilation and Distribution
Sequence Sciences offers meticulous central lab manual compilation and distribution services to support clinical trial sites. Our team ensures that all protocols and procedures are clearly documented, standardized, and easily accessible, minimizing inconsistencies across study locations. With streamlined distribution processes, we make certain that every site receives the necessary materials on time, supporting compliance and reliable trial execution.
Site Training
Sequence Sciences delivers comprehensive site training to ensure that all study teams are fully prepared and knowledgeable on trial protocols. We provide customized training sessions that cover specific procedures, data collection methods, and compliance requirements tailored to each trial’s unique needs. Our approach fosters consistency and accuracy across all sites, enhancing the reliability of trial outcomes and promoting regulatory adherence.
Sequencing
Targeted and non-targeted, custom de novo bionalytical asssay development, and modeling.
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