Decode your clinical data with compliance for better analysis.
Code your way through the complexity of your clinical studies
to derive insights in a streamlined process at scale and speed.
Essential for pharma, biotechnology, life sciences, and nutraceutical industries.
Enables accurate analysis and interpretation of clinical data.
Evaluates efficacy and safety of drugs and medical devices.
Supports diverse study types including parallel, crossover, multi-phase, PK/PD, and real-world evidence.
Strong team of experienced statistical programmers.
Specialized in supporting clinical trials of all sizes and therapeutic areas.
Accurate, on-time analysis of clinical trial data.
Ability to work with both standard formats and sponsor-specific templates.
Creation and Quality Control (QC) of regulatory submission-ready analysis datasets.
Production of Tables, Listings, and Figures (TLFs) for data presentation.
Independent quality control for datasets and TLFs to ensure accuracy before biostatistician review.
Conversion of heterogeneous data into a unified metadata model for streamlined evaluation.
Outputs aligned with SOPs, ICH, and other regulatory guidelines.
Stringent and streamlined processes to maintain efficiency.
Collaboration between statistical programmers and biostatisticians for precise results.
Flexible reporting — from our standard templates to fully customized sponsor-specific formats.
IQA’s statistical programmers will meet every statistical need including the creation and QC of regulatory submission-ready analysis datasets and the production of TLFs (Tables, Listings, and Figures) working closely with our Biostatistics team. Further, we conduct quality control for analysis datasets and TLFs independently to make sure biostatisticians receive accurate results for final review.
At IQA, we have established a stringent and streamlined process to enable our team to convert heterogeneous data into unified metadata model to create TLFs for easy evaluation of efficacy and data integrity. Our outputs are in line with regulatory guidelines including SOPs and ICH. Moreover, our team is highly flexible in generating any types of reports whether based on our standard format or sponsor-specific templates.
IQA Statistical Programming services include many ad hoc analyses for publication summaries and external/internal review meetings. Also, you get access to a team that is adaptable to industry changes, implementing latest advances in compliances, standards, technology, and industry requirements for efficient clinical data handling.
Let us help you manage criticalities and compliances of processing volumes of clinical trial data through efficient programming models.
