Welcome to the flexible, no-nonsense Dutch CRO, ready to process your clinical study data
FOUR TIMES FOUR TOP REASONS TO CONTACT US!
Leading Expertise
- Highly experienced CDISC-knowledge with FDA-compliant data output, including SDTM, ADaM, and define.xml
- Superb specified statistical support
- Easily integrable and bookmarked TLF output
- Using the latest technologies to get your study data submission-ready, including SAS Analytics Pro on Viya and R programming
IF NOT CONVINCED YET, KEEP READING!
Core Standards
- We move as a team together with your company and demands. Read about us.
- We work in a highly standardized way, aiming for cross-platform and root folder-independent compatibility
- We improve the process efficiency by advising on the whole data collection to submission process
- We keep an eye on quality and timely delivery, preferably by four!
ALL-ROUND SUPPORT!
Enhancing your environment
- Standardizing your controlled programming environment
- Supporting your programming protocols
- Assist in MS Office automation, including macro-driven templates and custom toolbars
- Assist in scientific publications
EVEN MORE REASONS ..!
What we value
- Personal approach and engagement, we care about our clients
- Affordablity, we also care about the patients and would love to see that good products get marketed
- Flexibility, we know that product development changes over time
- Combining forces to create transparent, and regulatory authority compliant output
