Statistical Analysis
ADI Intellect's Expert Statistical Analysis Services
At ADI Intellect, we understand the importance of extracting meaningful insights from data to drive informed decision-making and advance knowledge in various fields. Our team of expert statisticians and data analysts is acquainted with CDISC and can put together a CDISC strategy that meets organizational, monetary, and regulatory targets. We have created datasets for several SDTM, ADaM, and CDISC-compatible studies and completed numerous CDISC-compliant regulatory filings.
The Right Expertise for
Your Study
Clinical Trials
We provide statistical analysis support for clinical trials, including data management, analysis, and reporting using Clinical SAS.
Therapeutic Areas
Our team has expertise in various therapeutic areas, including oncology, cardiology, neurology, and more.
Pharmacological Progression
We support the drug development spectrum, from initial discovery to approval, with our statistical analysis services.
Accelerate Breakthrough Treatments with Our Expertise
Our team of experts has extensive statistical methods experience in:
SAS Programming: We provide expert clinical SAS programming services to manage and analyze your data.
Macro Production, Validation, and Optimization: We develop and optimize macros to streamline data processing and analysis tasks.
Interim Analysis Support: We provide temporary examination assistance for interim analyses in clinical trials.
CDISC Mapping/Conversion Capabilities: We map and convert data to CDISC standards, ensuring compliance with regulatory requirements.
CDISC Submission-Ready Dataset Development and QC: We develop and quality-check CDISC submission-ready datasets to ensure compliance with regulatory requirements.
Analysis Datasets and TLFs Development: We develop analysis datasets and TLFs to support your research study or clinical trial.
Define.xml Files for SDTM and ADaM: We create Define.xml files for SDTM and ADaM datasets, ensuring compliance with CDISC standards.
Submission-Ready Packages: We develop submission-ready packages, including Define XML, Reviewer’s Guide, and Analysis Metadata, to support your regulatory submissions.
Why Choose ADI Intellect For Statistical Analysis Plan?
With our support, you can :
- Leverage our comprehensive understanding of drug development phases
- Tap into our expertise in multiple therapeutic areas
- Meet regulatory approval deadlines with submission-ready deliveries
- Ensure high-quality services that meet industry standards and regulatory requirements.
Together, let’s drive innovation and bring groundbreaking treatments to those who need them most.