SAS Biostatistics Support
Expert Analysis for Clinical Trials and Academic Research
Leverage the power of SAS for your research with our expert support. At Thesis Writing Cafe, our team of certified SAS programmers and biostatisticians provides comprehensive services for clinical trials, academic theses, and pharmaceutical research, ensuring your data analysis is accurate, compliant, and robust.
SAS Certified Programmers
CDISC Compliant
100% Confidential
Our SAS Biostatistics Services
Why Choose Our SAS Experts?
Industry & Academic Expertise
Our team has deep experience in both the pharmaceutical industry and academic research, understanding the unique demands of each.
Regulatory Compliance
We are experts in the statistical requirements for regulatory submissions to bodies like the FDA, EMA, and CDSCO.
Focus on Quality and Accuracy
Our rigorous quality control process ensures that all programming and analysis are accurate, validated, and reliable.
Efficient & Timely Delivery
We understand the importance of timelines in clinical trials and academic research and are committed to on-time delivery.
Clear Documentation
All our work is delivered with clear, well-commented code and comprehensive documentation for transparency and reproducibility.
Flexible Engagement Models
We offer flexible support, from hourly consulting to full-service project management, to meet your specific needs.
Our 4-Step Process
Submit Requirement
Share your research area and specific needs through our consultation form.
Get Quote & Plan
Receive a customized plan and a detailed quote for your project.
Collaborate with Expert
Engage in one-on-one sessions with your dedicated academic mentor.
Receive & Review
Get your completed chapters, provide feedback, and request revisions.
Our Authoritativeness & Recognition
Thesis Writing Cafe is a registered and verified business, recognized on major international platforms for our commitment to quality.
Frequently Asked Questions
What SAS procedures do you have expertise in?
Our SAS experts are proficient in a wide range of procedures, including but not limited to PROC GLM, PROC MIXED, PROC LOGISTIC, PROC PHREG for survival analysis, and various data management procedures within SAS Base and SAS/STAT.
Can you help with CDISC standards (SDTM and ADaM)?
Yes, our team has extensive experience in creating and validating CDISC-compliant datasets, including SDTM (Study Data Tabulation Model) and ADaM (Analysis Data Model), which are essential for regulatory submissions.
Do you provide support for both academic and industry projects?
Absolutely. We provide tailored SAS biostatistics support for academic researchers (PhD and Master’s theses), as well as for pharmaceutical companies, CROs, and other industry clients conducting clinical trials and health research.
What Our Clients Say About Our SAS Support
“The SAS programming and analysis for our clinical trial data were impeccable. The team’s expertise in CDISC standards and regulatory requirements was a huge asset. Highly professional service.”
“I needed help with a complex mixed model analysis in SAS for my PhD thesis. The consultant was incredibly knowledgeable and provided clear, well-documented code and a thorough interpretation of the results.”
“Their team reviewed our statistical analysis plan and provided invaluable feedback that strengthened our study design. Their understanding of SAS and clinical trials is top-notch.”
Our Location
Need Expert SAS Biostatistics Support?
Ensure your analysis is accurate, compliant, and ready for publication or regulatory submission. Contact us for a free, confidential consultation.