We operate as a specialist CRO with a proven track record of excellence in designing, managing, and executing Clinical Trials, Expanded Access Programs, and Commercialization Solutions across the globe.
We are experienced in Phase I – IV trial delivery with proven track record of excellence supporting 60+ clinical programmes worldwide.
Define Research Objectives & Hypothesis
Develop Study Protocol
Secure Funding & Resources
Regulatory & Ethics Approval Support
Country Selection for Research Sites
Patient Feasibility and Site Selection
Site Set-Up & Contracting
Vendor Selection & Management Support
Interactive Response Technologies
Drug Supply Management
Data Management Plan
Safety Management Plan
Medical Monitoring Plan
Training Investigators & Site Staff
Pre-Trial Clinical Research Site Visits & Compliance Checks
Identify Eligible Participants
Screen & Enroll Eligible Participants
Site Support & Management
Patient Retention Strategies
Patient Concierge Service
Nursing Services
https://www.wepclinical.com/cro/trial-execution-monitoring/project-management/
https://www.wepclinical.com/cro/trial-execution-monitoring/site-monitoring/
https://www.wepclinical.com/cro/trial-execution-monitoring/drug-safety-pharmacovigilance/
https://www.wepclinical.com/cro/trial-execution-monitoring/medical-monitoring-support/
https://www.wepclinical.com/cro/trial-execution-monitoring/quality-control-and-assurance/
https://www.wepclinical.com/cro/medical-affairs/
https://www.wepclinical.com/cro/medical-writing/
https://www.wepclinical.com/cro/regulatory-affairs/
https://www.wepclinical.com/cro/data-management-analysis/data-cleaning-validation/
https://www.wepclinical.com/cro/data-management-analysis/statistical-analysis/
https://www.wepclinical.com/cro/data-management-analysis/data-compliance-submission/
https://www.wepclinical.com/cro/study-close-out-reporting/post-marketing-surveillance/
Close-Out Site Visits and Audits
Final Report Submission
Clinical Trial Publications
Post-Marketing Surveillance
Industry leader with over 16 years of experience designing and delivering value-driven Expanded Access (EAPs) and Post-Trial Access Programs.
As an industry-leading provider we help ease the burden placed on all study stakeholders by allowing patients to participate in clinical trials from the their homes.
Data Management Plan Trial Initiation Home / Page We understand that robust data management is critical to the success of your clinical trial. A well-structured Data Management Plan (DMP) serves as the foundation for ensuring
