EN 
DE Targeted clinical research for pharma and medicine sector
We plan, monitor and check.
For safe and effective medicines and medical devices.
Highest
safety standards
Efficient
study administration
TÜV certificate
EN ISO 9001:2015
Time pressure, costs and high requirements?
Are you worried about the compliance with legal requirements in your studies ?
Are you looking for a reliable partner who can handle your studies efficiently and cost-effectively ?
Do you need support to turn your results into usable data for the market ?
We accompany you through all phases of clinical trials – from first use to post-authorization surveillance. With our expertise, we ensure that your studies are safe, efficient and compliant. Through close cooperation with doctors and clinics we provide precise data that supports the success of your drugs and therapies on the market. Trust CW-R&M as your partner for reliable and goal-oriented study implementation.
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.
Your contact and managing director:
Christian Wolflehner
Exceeding Expectations: Proactive Approaches for On-Time Results
Discover how CW-Research & Management optimizes your clinical studies! With locations in Austria and Germany we combine regional expertise with international know-how. Our dedicated team offers flexible, tailor-made solutions and ensures that you are always well informed.
Benefit from over 30 years of experience and a proactive approach that responds to your needs. Learn more about our innovative services and how we can help you achieve your goals!
Guidebook
How do I find suitable patients for clinical trials?
Finding patients for clinical trials is challenging and often time-consuming. But don't worry: We will help you recruit suitable participants efficiently.
How can I reduce the costs of clinical trials?
Clinical trials are expensive, especially for smaller companies. But how can costs be reduced without compromising on quality or safety?
What regulations do I have to follow for drug studies?
Clinical trials are subject to strict regulations such as GCP, AMG and GDPR. But how can all regulations be implemented reliably, safely and efficiently?