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Clinical SAS

Clinical SAS
Experienced bio-statisticians can provide expert opinion and help you make critical inferences and decisions from your clinical trial operations. Our clinical programming and bio-statisticians team is the largest department within Hezemon and its global reach offers great flexibility for our customers. Our experienced programmers have detailed knowledge of all Phases and all therapeutic areas across the drug development spectrum making them an ideal fit with existing project teams at client sites or to form the basis of new teams.
Our clinical programmers are industry leaders in providing validated results to clinical study reports and submission ready deliverables.
Hezemon team also offer support in electronic submissions, S-Plus Programming and process development (including Software Development Life Cycle).
Services
SAS Programming
Programming based on analysis data
Independent quality reviews
Customized clinical data outputs
Proactive, results-oriented approach to programming
Adoption of sponsor’s programming (SOP) Preparation of Case Report Tabulations (CRT) for submission
Programming based on data validation plan
Programming of TLFs for clinical study report and data monitoring committee
SDTM Mapping
CDISC-ADAM
Bio-statistics

Consultation on study design
Protocol development
Randomization
Statistical Analysis Plan (SAP)
Interim analysis
DSMB participation
Sample size calculations

Contact Email ID: info@hezemon.com
Visit: www.hezemon.com
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