Need submission-Ready Data?
Our Services
SEND DATASETS
Creation of Standard for Exchange of Nonclinical Data (SEND datasets) to regulatory submissions. We develop submission ready SEND datasets compliant with SENDIG v3.0/3.1/3.1.1, DART 1.2 and SENDIG-GeneTox v1.0
SDTM Mapping
Clinical study raw data mapped to SDTM for all trial phases (I to IV).
Generation of Study Data Tabulation Model (SDTM) datasets for clinical trial data submission
Clinical TLFs
Regulatory-quality Tables, Listings, and Figures generated using validated SAS macros and submission-ready formats
ABOUT US
“Your Partner in Regulatory Data Excellence.”
Cyprus, founded in 2018, is a specialized data services company focused on delivering high-quality, regulatory submission-ready datasets for preclinical and clinical research. With a strong foundation in global data standards such as SEND, SDTM, and ADaM, Cyprus supports pharmaceutical, biotech, and CRO clients in achieving compliance with evolving regulatory requirements. Backed by years of industry experience and a commitment to quality, we ensure accurate, audit-ready data packages tailored to agency expectations
QUESTIONS?
Whether you’re curious about services or free demo, we’re here to answer any questions.