TxScape(TM)
Proprietary Line of therapy (LOT) diagnostic and validation package for solid tumor and hematologic cancers
Ensuring precise exposure in real-world research is crucial yet frequently disregarded. Our comprehensive and iterative regimen development package is designed to guarantee a robust and scientifically validated study exposure. Let us help you achieve optimal exposure algorithms for your studies.
CDISC Conversion
Conversion Tool to Meet FDA Data Standards for Regulatory Submissions
Are you preparing observational studies for regulatory submissions but your data isn't in the right format? FDA mandates that real-world data for regulatory submissions must adhere to CDISC SDTM and ADaM standards. Let us convert and package your real-world data to meet these requirements and assist you in the submission process.
Regulatory Staging(TM)
Proprietary package to set up regulatory grade environments for regulatory-grade RWD studies.
Do you need to conduct regulatory-grade study for submission to authorities like FDA or EMA but don't have your environment set up? We specialize in setting up a regulatory-grade framework and checklist for your current study and future endeavors. Let's ensure your study meets all the necessary requirements.
EpiInsights(TM)
For Tailored Data Solutions
Are you a data partner that seeks assistance in effectively marketing your data to your targeted audience? We meticulously evaluate your data, emphasize its strengths, highlight key differentiators, and conduct gap analysis to tighten your data. Our customized packages are designed to enhance data visibility for your clientele.
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