Envision Research can connect sponsors and CROs with qualified physician investigators to successfully and effectively conduct clinical trials.
Why choose Envision Research?
Envision Research can
- Connect you with physician practices to conduct clinical trials, including but not limited to oncology, neurology, dermatology, internal medicine
- Provide infrastructure and resources needed for clinical trials
- Provide feasibility assessment, contracting and budgeting, regulatory and Institutional Review Board (IRB) Management, study-specific site training, data management, a Clinical Trials Management System (CTMS), Standard Operating Procedures for quality assurance, patient recruitment strategy, marketing, and adherence to Good Clinical Practice (GCP) and quality control
How Envision Research Operates
- Streamlined intake process for clinical research projects
- Strategic support from CDA to Close-out.
Clinical Trial Management
- Certified and skilled clinical research and regulatory coordinators
- Professional, friendly and communicative interactions with sponsors, CRO staff, PIs, clinical site staff, and patients.
- Over 20 years of expertise in budgeting, contracting and management expertise in clinical research allows Envision Research to provide fast responses to sponsors in alignment with industry standards.