Programming
Experienced Programming Support for All Your Clinical Trials Needs with Data Management and Biostatistics
Ergomed offers a full range of nonstatistical and statistical programming services for clinical trials across all phases, noninterventional studies, and retrospective data analyses. Our Electronic Data Capture (EDC) developer team is expert in building custom EDC solutions to optimize trial efficiency and cost-effectiveness. Our team of Statistical Analysis Software (SAS) programmers provides support to data management programming needs like data reconciliation or editing checks. And our statistical programmers are experienced across most therapeutic areas with specialist experience in oncology and rare disease for all your data analysis and tabulation needs.
Data Management Programming
At Ergomed, we offer specialized Clinical Data Management (CDM) programming services designed to meet the highest clinical research standards. Our focus on quality, accuracy, and efficiency ensures reliable outcomes for your clinical trials.
Statistical Programming
Our statistical programming team is located across the EU and India and has, on average, ten years of industry experience. They are experts in SAS and apply their skills across a wide range of tasks, from simple data listings to support medical review to a submission-ready package of CDISC datasets and supporting documentation, all using best practices and the latest implementation guides. Robust processes set the team up for success with a special emphasis on first-time quality while offering flexibility to the needs of our unique and diverse customer base. The team also has a solid statistical background to provide robust analytical support throughout the research process, working very closely with their colleagues in Biostatistics.
Our key services include, but are not limited to:
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Continuous programming support throughout the trial to aid data review and quality for a smooth database lock.
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Developing domains that are Clinical Data Interchange Standards Consortium (CDISC) compliant using Study Data Tabulation Models (SDTM) and Analysis Data Models (ADaM), with complete documentation and validation.
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Comprehensive analysis and detailed reporting of clinical trial data, ensuring clarity and accuracy in presenting results.
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Creating comprehensive and informative tables, listings, and figures to communicate study findings effectively.
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Providing programming support (e.g., data listings, patient profiles) to ensure ongoing safety reviews are conducted to aid in the identification of any safety concerns, trends, or general issues with the data during the study.
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Expertise with Phoenix WinNonlin to take concentration data and derive pharmacokinetic parameters to support statistical summaries and analyses to understand drug behavior.
Programming Expertise Tailored to Your Clinical Trial Success
Ergomed’s programming services are meticulously designed to support every aspect of your clinical trials with precision and efficiency. Our dedicated teams of EDC developers and SAS programmers are committed to delivering custom solutions that enhance trial outcomes and streamline processes. Whether you need robust data management programming or comprehensive statistical analysis, our experts are equipped to handle the complexities of clinical research, ensuring high-quality results and adherence to industry standards.
Partner with us to leverage our extensive experience across therapeutic areas, including oncology and rare diseases, and confidently achieve your clinical trial objectives. Contact us today to discover how Ergomed’s programming expertise can drive the success of your subsequent study.
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