Quality Clinical Trial Management Services
Quality Clinical Trial Management Services
The following services either on an ad-hoc, limited contract or fully insourced basis by using our systematic and client centric BEAVER Methodology
- Site Management Organization
- Clinical Monitoring and Clinical Monitoring Program
- Audits and Audit Management Program
- Development of CRFs, Protocols, Informed Consent Forms
- Quality Review of Clinical study data
- Translation services
- Document Archival Services
- Pharma-Clinical Research Industry Legal Contract / Agreement Management services
BEAVER Methodology: Our Clinical Research services are basically a six-step systematic, client centric process in order to provide innovative industrious, cost-effective, quality and timely services.
Step 1
Broaden understanding of Client study design and requirements.
Step 2
Evaluate potential unique strategies, risk-based quality approaches for the study design and conduct opportunities.
Step 3
Assess the quality of study design, resources and quality management system.
Step 4
Vow to create and use a metrics that measure study’s efficacy and safety endpoints, and overall performance of the study.
Step 5
Engage with Clients and BEAVER study team and other SMEs time to time
Step 6
Reinforce interest in the Client proposals by consistently and persistently following up with the right decision makers.