WEP CRO Built for Biotech

We are experienced in Phase I – IV trial delivery with proven track record of excellence supporting 60+ clinical programmes worldwide.

  • Research Objectives
  • Study Protocol
  • Funding & Resources
  • Regulatory & Ethics Approval
  • Country Selection
  • Feasibility & Site Selection
  • Planning and Preparation
  • Site Set-Up & Contracting
  • Vendor Selection
  • IRT
  • Drug Supply Management
  • Data Management Planning
  • Safety Management Planning
  • Medical Monitoring Planning
  • Site Training
  • Pre-Trial Site Visit
  • Study Startup
  • Patient Identification
  • Screening & Enrollollment
  • Site Support & Management
  • Patient Retention Strategies
  • Patient Concierge Service
  • Nursing Services
  • Patient Recruitment & Retention
  • Project Management
  • Site Monitoring
  • Drug Safety & Pharmacovigilance
  • Medical Monitoring
  • Quality Control and Assurance
  • Medical Affairs
  • Medical Writing
  • Regulatory Affairs
  • Clinical Support services
  • Global Operating Model
  • Patient Centric Approach
  • Nurse Training
  • Clinical Trial Nursing
  • Data Cleaning & Validation
  • Statistical Analysis
  • Data Compliance & Submission
  • Data Management
  • Data Management & Analysis
  • Close-Out Site Visits and Audits
  • Final Report Submission
  • Clinical Trial Publications
  • Post-Marketing Surveillance
  • Study Close Out & Reporting