Clinical programming
Automate clinical data for faster & streamlined analysis
Automate your way to a successful clinical trial by programming data transformation, integration, and analysis producing comprehensive reports
Clinical programming is the process of automating the analysis and interpretation of clinical trial data through programming. With IQA’s services you can get the best of both human minds and technology to analyze your clinical data and generate insightful reports. Our processes are in accordance with industry standards and regulatory requirements including CDISC.
Our clinical programming team is capable of catering to all your needs right from database design to creating analytical and reporting dashboards as we generate datasets in unified metadata models like SDTM and ADaM. We focus highly on quality and integrity of our work while saving time and cost for you.
As a trusted partner to provide clinical programming services, IQA designs innovative programming solutions tailored to suit your clinical study specification helping you to effectively analyze and represent the data collected during the trials validating accuracy and efficiency.
We use cutting-edge technology and emerging software techniques to strengthen our services that are run by a team of expert clinical programmers with extensive experience in multiple programming languages including SAS, R, and Python
Trial Insights
IQA clinical programming services include near-real-time reporting with an overview of data insights like biomarker read-outs and preliminary efficacy trends. The reports shared in a visually appealing manner will equip you with
- Insightful trends and patterns
- Enhanced decision-making process
- Seamless DMCs, DSMBs, protocol amendments
- Other development plans
We provide you with complete transparency through end-to-end visibility into the state of your clinical research.
Our core competency includes
Ensure success of your clinical trial with our programming support
Outsource the complexity of data analysis and programming to us while you progress your clinical trials with confidence.