Welcome to the flexible, no-nonsense Dutch CRO,
ready to process your data
FOUR TIMES FOUR TOP REASONS TO CONTACT US!
Leading Expertise
- Highly experienced in regulated industry, including pharma, exteding to medical devices, and biotech data submissions
- Up-to-date and detailed CDISC-knowledge to create SDTM, ADaM, and define.xml FDA-compliant output
- Superb specified statistical support from data analysis to easily integrable and bookmarked TLF output
- Using the latest technologies including SAS Analytics Pro on Viya and R programming, to get your data in shape
Talk to us about your needs in data analysis and standardization support. We are available for different industries and for semi- and non-commercial organizations.
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 care about patient, customers, and individuals and are more than happy to support your good initiative
- Flexibility, we know that product development changes over time
- Combining forces to create transparent, and regulatory authority compliant output
