Planning & Preparation

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Planning & Preparation Trial Initiation Patient Recruitment, Enrollment & Retention Trial Execution & Monitoring Data Management & Analysis Study Close Out & Reporting

Laying the foundation for clinical trial success

At WEP we believe that a well-structured clinical trial begins with meticulous planning, which is essential for designing a scientifically sound and regulatory-compliant study. Our expertise in early-stage trial planning enables Sponsors to navigate complex regulatory landscapes, streamline processes, and anticipate potential challenges.

By optimizing timelines and implementing effective risk mitigation strategies, we ensure a smooth and efficient clinical journey. Our commitment to thorough planning helps maximize the trial’s success and deliver meaningful, reliable results.

Key tasks

Define Research Objectives & Hypothesis

With decades of clinical research experience, deep therapeutic understanding, and a commitment to patient-centered drug development, WEP is ideally positioned to help Sponsors define research questions, refine hypotheses, and develop study designs that are scientifically valid, feasible, and aligned with regulatory expectations.

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Develop Study Protocol

We understand that a well-structured and comprehensive study protocol is the foundation of a successful clinical trial, guiding every stage of execution from site selection to patient recruitment and data collection. Our team supports Sponsors with study protocol development, ensuring scientific rigor, regulatory compliance, and operational efficiency.
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Secure Funding & Resourcess

WEP’s experienced team can assist Sponsors in securing essential funding and efficiently allocating resources necessary for clinical trials and research programs. By leveraging our expertise, WEP helps develop realistic budgets, optimize financial planning, and design cost-effective trial strategies. Their tailored approach ensures resource optimization, maximizing the chances of successful project outcomes.
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Regulatory & Ethics Approval Support

We provide comprehensive global regulatory expertise to help Sponsors navigate the complex and ever-evolving landscape of clinical trial regulations. Our team of seasoned experts coordinate all aspects of the regulatory process, across every stage of the development journey, providing true end-to-end support. We leverage decades of experience and utilize data-driven strategies to maximize study success.
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Country Selection for Research Sites

Selecting the right countries for a clinical trial is one of the most critical factors influencing the success, speed, and cost-effectiveness of the study. Poor country selection can lead to delays, regulatory hurdles, recruitment failures, and increased costs, while an optimized strategy can accelerate approvals, improve data quality, and enhance patient diversity.
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Patient Feasibility & Site Selection

Effective site selection is vital for a clinical trial’s success, while patient feasibility assessments ensure successful recruitment and retention. WEP uses a comprehensive, structured approach to identify and select sites and patients strategically, maximizing the trial’s ability to meet recruitment targets and achieve successful outcomes.
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Meet The Team.... TBC

Sara Parker

Kitchen Chronicles

About Me

I combine my love of food and storytelling to create beautiful photos.

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