Intensive monitoring and quality oversight programs supported by a unified technology system.
Uncompromising quality and accurate data delivery
Velocity has created a unique, industry-leading quality oversight model. All Velocity sites and studies are supported by in-house clinical data, quality assurance, regulatory, and risk management teams.
These veteran teams work directly with site staff, serving as a resource to help identify — and leverage — areas for continuous improvement. The teams support all aspects of QA/QC processes to ensure adherence to all applicable FDA regulations, ICH GCP Guidance, state guidelines, industry standards, and Velocity's stringent SOPs.
- 48-hour data entry target; query resolution within 48 hours of generation
- Routine and random QA reviews; EDC and source cross-checks
- Commitment to the routine investigator and site staff training
- CLIA-certified labs, IATA-certified staff, GCP-trained physicians and staff
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