SAS Programming
We provide comprehensive programming solutions, including dataset creation, statistical analysis, ADaM dataset generation, and TLF production. Our commitment to quality and adherence to industry standards ensures that your clinical trials run smoothly and your data meets the stringent requirements of global regulatory bodies. Whether you’re in early development or post-marketing phases, our SAS Programming services support your clinical journey from start to finish
What we do?
Our expertise ensures precise, reliable data that guides your product from early stages to post-approval
Statistical Analysis
Conduct comprehensive statistical analyses using advanced SAS techniques. Our analyses support robust decision-making and meet regulatory requirements for submissions
ADaM Dataset Generation
Create ADaM datasets to facilitate efficient and accurate statistical analysis. Our meticulous approach ensures data traceability and regulatory compliance
Data Validation and QC
Implement rigorous validation and quality control processes to ensure the accuracy and integrity of your data. Our thorough checks reduce the risk of errors and enhance data reliability
Regulatory Submission Support
Prepare and review SAS datasets and outputs for regulatory submissions, ensuring they comply with FDA, EMA, and other global standards. Our expertise facilitates a smooth submission process
Custom Programming Solutions
Develop bespoke SAS programming solutions to address unique study requirements. Our flexible approach adapts to the complexities of your clinical trial data
Data Integration and Standardization
Integrate and standardize data from multiple sources into cohesive SAS datasets. Our expertise ensures consistency and facilitates cross-study comparisons and meta-analyses
Our Differentiators
Our expertise ensures precise, reliable data that guides your product from early stages to post-approval
Customized Solutions
We offer tailored SAS programming solutions that address the unique requirements of your clinical trials, from simple studies to complex, multi-center projects
Comprehensive Quality Control
Our multi-layered quality control processes ensure data accuracy, completeness, and integrity, minimizing the risk of errors and ensuring reliable data for decision-making
Seamless Integration
Expertise in integrating data from diverse sources, including EDC systems and legacy databases, into cohesive SAS datasets that support comprehensive analysis and reporting
Holistic Approach
Deliver end-to-end SAS programming services that cover the entire clinical data lifecycle, from early development to post-marketing, ensuring consistent, high-quality data management and analysis
Our success based on how happy our clients are
As a full-service CRO, we specialize in clinical development, post-marketing,
and functional service support, ensuring your projects are managed with precision and integrity
Hira Technologies has been instrumental in the success of our clinical trials. Their expertise, responsiveness, and commitment to quality have kept our projects on track and within budget. Highly recommend for clinical development needs.”
Chief Medical Officer
Biopharma Company
Hira Technology’s post-marketing support has been crucial for our product’s success. Their proactive monitoring and detailed reports ensure compliance and inform our market strategy. Exceptional service and expertise.”
CRO
Pharma Company
Partnering with Hira Technologies for functional service support has streamlined our R&D operations. Their expert team integrates seamlessly with ours, delivering top-notch data management and biostatistics services. Outstanding professionalism.”
Head of R&D
Biotechnology Firm