Acceler8 Clinical Monitoring

Acceler8 Clinical Research

Acceler8 Clinical Monitoring

Clinical monitoring and site management services delivered by our in-house CRAs

Clinical Surveillance

Do you know anyone using Acceler8 Clinical Monitoring?

Our experienced CRAs support global and regional clinical trials through our comprehensive suite of clinical monitoring and site management services, from feasibility through to site closeout.

Feasibility Assessment

  • Study feasibility assessment

  • Country/Site recommendations

Site Identification and qualification

  • Site assessment

  • Review staff/investigator credentials

  • Collate documentation

Investigator Site Set Up & Initiation

  • Briefing/training of investigators, sub-investigators and staff

  • Initiation in study procedures and documentation

Site Management

  • Recruitment planning/tracking

  • IMP Management

  • Query resolution

Site Monitoring

  • Review of source data, recruitment, informed consent, CRF, investigator site file

Auditing

CQA Site audits are delivered by our CQA team

Site Closeout

  • Ensure completeness of study documentation

  • Closeout agreement and report

Acceler8 Clinical Monitoring

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