Services
Why Choose AfriTrials Connect
At AfriTrials Connect, we understand the critical role of a quality feasibility assessment in identifying suitable sites, assessing adequate patient populations, understanding the regulatory landscape, mitigating risks, estimating realistic timelines and costs, thereby eliminating potential delays
Our approach is built on three pillars:
- Data-Driven Insights: We provide actionable intelligence to simplify decision-making
- Efficiency and Speed: We deliver feasibility assessments in record time, helping you accelerate timelines
- Our deep understanding of Africa’s clinical research ecosystem ensures unmatched reliability and results
Our Services
At AfriTrials Connect, we’re redefining how clinical trial site feasibility is conducted
Site feasibility assessment
- Tailored insights into site capabilities, ensuring compliance and operational capacity
Robust Database Access
- A growing network of verified clinical trial sites across Africa
Consulting Services
- Expert support in navigating the regulatory landscape, ensuring smooth trial setup
Collaboration Opportunities
- Connecting sponsors, CROs, and research institutions to foster innovation and growth
- Subscriptions: Monthly or annual plans for platform access
- Custom Reports: Tailored feasibility studies on specific regions and conditions
- Consulting: Advisory services for trial site selection and regulatory navigation
Benefits Of Saving Cost and Time For Sponsors In Performing Site Feasibility and Evaluation
At AfriTrials Connect, we understand the critical role of a quality feasibility assessment in identifying suitable sites, assessing adequate patient populations, understanding the regulatory landscape, mitigating risks, estimating realistic timelines and costs, thereby eliminating potential delays
Faster Trial Start-Up
- Quicker Decision-Making: Efficient site feasibility and evaluation processes allow sponsors to select sites more quickly, accelerating the overall trial timeline
- Earlier Patient Recruitment:> By identifying sites ready to start immediately, sponsors can initiate patient recruitment sooner, reducing delays in trial progression
Cost Efficiency
- Improved Trial Success Rates
- High-Quality Data Collection: Thorough feasibility studies ensure sites have the necessary infrastructure and expertise, resulting in accurate and reliable data
Reduced Site Attrition
- Identifying capable sites during the feasibility stage minimizes the risk of sites dropping out mid-trial, which can disrupt timelines and increase costs
Enhanced Compliance and Risk Mitigation
- Regulatory Readiness: Evaluating sites for compliance with local regulations reduces the risk of trial disruptions or penalties
- Lower Risk of Non-Performance: In-depth evaluations help identify sites that might lack resources or experience, avoiding costly mid-trial adjustments
Increased Sponsor Confidence
- Transparency: Access to detailed site feasibility data builds confidence in the trial’s operational plan
- Streamlined Collaboration: Sponsors can build stronger relationships with CROs and sites when feasibility studies establish clear expectations upfront
Competitive Advantage
- Speed to Market: Faster site selection and trial execution enable sponsors to bring products to market more quickly, capturing market share and generating earlier revenues
- Improved Reputation: Sponsors known for running efficient, well-organized trials attract more collaborations and opportunities in the future
