EN 
DE Responsibility instead of Volume +
Governance instead of Promise =
Reliable implementation instead of Planning optimism
Successful clinical trials require competent management, realistic timelines, and a clear oversight structure. As an experienced implementation partner, CW-Research & Management ensures that these factors work together reliably in your studies.
Highest
safety standards
Efficient
study administration
TÜV certificate
EN ISO 9001:2015
Who we are
CW-Research & Management is an independent European CRO with a strong regulatory foundation and clear Governance orientation in Research and Development. We provide comprehensive advice, monitor the study implementation, analyze data and define targeted strategies and methodological approaches together with you.
In an increasingly complex regulatory environment, we therefore support sponsors not only operationally, but also structurally and actively in the planning and execution of clinical trials.
Tailor-made solutions for your challenges:
Ensure efficient study planning
➤ Study planning
Individually coordinated plan for compliant implementation.
➤ Risk management
Early detection and prevention of potential risks.
➤ Project management
Structured and timely implementation.
Ensure safety and quality
➤ Monitoring
Continuous monitoring for maximum safety.
➤ Quality assurance
Regular independent audits for compliance.
➤ Medical writing
Data from trusted and verified sources, correctly interpreted.
Precisely evaluate complex data
➤ Data management
Collection and organization of study data.
➤ Biometrics
In-depth analysis of the results.
➤ Coding
Structured preparation for clear results.
Achieve time and budget goals
➤ Project management
Efficient control for timely and cost-effective implementation.
➤ Quality assurance
Control measures to avoid delays.
➤ Risk management
Proactive minimization of time, cost and resource risks.
Study Governance & Oversight
➤ Sponsor Oversight Support
➤ Efficient Site Activation
➤ Inspection Readiness
➤ Audit Support
➤ Vendor Oversight
➤ Cross-border coordination
We make the crucial difference
empty not delete
Quality assurance through senior-led execution
Instead of working with changing project teams, you will work with experienced senior professionals throughout the entire process, from planning to implementation. This allows complex tasks to be solved efficiently and potential errors to be avoided.
Clear strategic focus through a governance-first approach
Regulatory requirements are not a mere formality for us, but rather a prerequisite for establishing stable study structures. Therefore, we clearly define guidelines, control mechanisms, and responsibilities right from the start of a study, ensuring that compliance requirements are met and all components are designed efficiently.
Goal-oriented and results-oriented through realistic planning
We don't sell optimistic scenarios; instead, we plan robust and realistic studies. From the outset, our planning incorporates factors such as time and resource management, the identification of potential risks and their proactive mitigation, as well as a realistic assessment of the feasibility of your studies and projects.
Streamlined processes without loss of quality through operational acceleration
A high error rate often goes hand in hand with an overloaded study design. We reduce all processes and requirements to the absolute essentials – without compromising the quality of your data and without sacrificing the safety of your participants. We identify operational bottlenecks early and take targeted countermeasures, especially during the critical phase of study activation.
Your contact and managing director:
Christian Wolflehner
Doubly motivated, clearly focused: What we stand for
As an implementation partner in clinical contract research, we meet these requirements through forward-looking and realistically planned studies, which are cost-effectively planned and executed by experienced teams with a hands-on mentality. We see our role not only in conducting studies, but also in ensuring their structural stability.
Furthermore, we strive to keep the study design as flexible as possible wherever feasible. This means that if adjustments become necessary during the study, they can be made without requiring a complete redesign.
Overall, we at CW-Research & Management (CWRM) stand for:
- C: Competence and Compliance
- W: Workflow and Workmanship
- R: Responsibility and Reliability
- M: Methodology and Monitoring
Twice as good. Clear in its execution. Gladly also on your behalf.
Guidebook
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