SAS Research Outsourcing Services

Our SAS research outsourcing services empower clinical, epidemiology, and health data teams with validated SAS programming, robust statistical analysis, and submission-ready reports for global compliance.

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Our SAS Research Capabilities

Our certified SAS programmers and senior biostatisticians deliver reliable data handling, advanced modeling, custom macros, and automation for complex clinical and public health research projects.

Types of SAS Research We Handle

Clinical Trial Data Programming
CDISC SDTM and ADaM Mapping
Statistical Analysis Plan Execution
Regulatory Submission Dataset Preparation
Descriptive and Inferential Statistics
Time-to-Event and Survival Analysis
Mixed Models and Repeated Measures
Bioequivalence and Bioavailability Studies
Pharmacokinetic and Pharmacodynamic Modeling
Safety and Efficacy Data Summaries
Data Quality Control and Validation
Data Mining and Pattern Recognition
Predictive Modeling in SAS
Health Outcomes and Real-World Evidence
Risk Factor Analysis and Forecasting
Longitudinal Data Analysis
Epidemiological Data Analytics
Data Visualization and Reporting Automation
SAS Macro Development
Interim Analysis and Adaptive Designs
Meta-Analysis Using SAS
CDASH and eCRF Data Integration
Regulatory Compliance Audits
Cross-Lab Validation of SAS Code
Publication-Ready SAS Output
Custom SAS Training and Support
Regulatory-Compliant SAS Reports
Data Integration Across Multiple Studies
Secure Data Handling and Archiving
Custom SAS Research Projects

Key Research Outsourcing Services Offered

Custom SAS Code Development
Advanced Statistical Modeling and Analysis
CDISC SDTM and ADaM Conversion
Data Cleaning, QC, and Reconciliation
PK/PD Data Analysis and Reporting
Clinical Trial Statistical Programming
Real-World Evidence Data Analytics
Risk Analysis and Signal Detection
Health Outcomes Research Support
Regulatory Submission Preparation
SAS Macro Creation and Validation
Automated Report Generation
Meta-Analysis and Systematic Reviews
Data Visualization Dashboards
Publication-Ready Figures and Tables
Stakeholder Presentation and Support
Confidential Data Handling and NDA
Interim Progress Reports and Data Snapshots
Workshops and Training in SAS
Post-Project Technical Consulting
IP and Patent Filing Support for Algorithms
Grant Proposal and Manuscript Assistance
Secure Data Backup and Archiving
Compliance with GCP, GLP, CDISC Standards
Cross-Lab Code Validation and Audit Support
Collaboration with CROs and Pharma
Long-Term SAS Programming Partnerships
Custom SOP Development for SAS Workflows
Regulatory Dossier Preparation
Market-Ready SAS Data Reports

Why Choose Us for SAS Research Outsourcing?

Our trusted biostatistics team, rigorous QC, and CDISC-compliant workflows ensure precise, reproducible, and regulator-ready SAS outputs for clinical and health studies worldwide.

Industries & Sectors We Serve

Pharmaceutical and Biotech Companies
Clinical Research Organizations (CROs)
Public Health and Epidemiology Units
Health Economics and Outcomes Research (HEOR)
Academic and Medical Research Institutes
Regulatory Affairs and Data Compliance Bodies

Customized SAS Solutions

We craft custom SAS programs, automate statistical workflows, and deliver robust, regulator-compliant reports tailored to your protocol and submission timelines.

Quality Assurance & Regulatory Compliance

Our SAS processes adhere to GCP, GLP, CDISC, and regulatory guidelines ensuring validated, audit-ready, and submission-compliant deliverables.

Case Studies & Client Success Stories

Discover how our SAS outsourcing has streamlined clinical data pipelines, enabled rapid trial submissions, and supported evidence-based healthcare policies. References available on request.

How It Works: Our Research Outsourcing Process

Requirement Gathering: Define data sources, analysis plan, and regulatory endpoints.
Proposal & Quotation: Provide custom code plan, timeline, and cost estimate.
Programming and QC: Develop, validate, and review SAS datasets and outputs.
Reporting: Deliver CDISC-ready datasets, tables, listings, figures, and reports.
Post-Project Support: Offer revisions, submission support, and long-term code maintenance.

Frequently Asked Questions (FAQs)

Q: Can you handle large multi-center trial data?
A: Yes — we specialize in high-volume, multi-site clinical data programming and QC.

Q: Do you ensure CDISC compliance?
A: Absolutely — we map all datasets to SDTM and ADaM standards as per FDA and EMA requirements.

Q: How secure is my data and code?
A: We ensure strict NDAs, secure servers, version control, and full data traceability.

Get Started / Request a Quote

Contact us today to discuss your SAS project and receive a tailored plan, timeline, and cost estimate aligned with your clinical or health data objectives.