Our Clients
Optimize clinical research outcomes with technology-driven comprehensive clinical biometrics services designed to meet the needs of small and medium pharma and biotech companies. Leveraging data engineering, data analytics, and AI, we maintain the highest quality standards for your clinical trial data.
Our biometrics services in clinical trials include excellent support in data interpretation, study design, and statistical analysis, enhancing the decision-making process. Scale up confidently, accelerate clinical trial timelines, and have enhanced data access with our top-notch clinical biometric solutions.
When it comes to converting raw data to SDTM format, some pharma companies don’t have efficient processes in place. The challenges often include inaccurate data elements mapping, maintaining consistency across various clinical studies, and complexities in the naming conventions of variables.
Leveraging our expertise in artificial intelligence and machine learning, we automate the process of SDTM mapping. This significantly reduces the manual work required to be performed by SAS programming teams. It also accelerates the process while ensuring that the data quality remains the same.
Our biostatisticians offer statistical inputs to clinical trial protocols when it comes to study design, optimizing clinical development plans. They provide inputs on various aspects like sample sizes, study objectives, endpoints, randomization and stratification. We specialize in eCRF design as well as statistical review of CSRs (Clinical Study Reports). Our services include tailored data programs and expert analysis to meet your goals right from the beginning of a clinical study to its completion.
Get timely and accurate clinical trial reporting with our cutting-edge statistical programming techniques and automations. We use R, Python, SAS, and other statistical programming tools to ensure you get accurate deliverables. Our wide array of statistical programming services comprise developing analysis datasets and quality control, developing tables, listings, and figures (TLFs) and quality control for ISE and ISS, crafting statistical analysis plan (SAP), providing clinical trial safety updates annually, interim analysis support, and regulatory submission support.
Our vast experience enables us to create customized clinical study designs that resonate with our clients’ research objectives. From single endpoint trial designs to more complex Bayesian adaptive study designs, we can recommend designs most suitable for you. Our team can develop clinical study protocols and plans as well as provide you the necessary support and knowledge to attain your specific business goals. Our clinical study design services include, but are not limited to, sample size calculations, selection and confirmation of endpoints, protocol writing and review, cost estimation, randomization, and CRF design.
Become CDISC compliant fast and cost-effectively with our CDISC services. Our team has vast experience of working on different CDISC specific projects, where we provided only consultancy for some and mapped various studies to CDISC standards for others. Under our CDISC services, we develop new databases that are CDISC CDASH/SDTM compliant, map clinical studies from legacy to CDISC standards for FDA submission and ISS/ISE reporting, and convert SAS datasets to CDISC ODM XML and vice versa.
We provide top-notch clinical data acquisition services in which we design and build robust databases that help to maintain quality and speed for both simple and complex clinical trials. The data capture systems we design are aimed at meeting the needs of the end user. Moreover, these data acquisition systems can gather real-time data from IoT and mobile devices, enhancing the effectiveness of clinical data analysis.
When technological prowess teams up with extensive domain experience and process best practices, it leads to unrivaled clinical data management. What gives us an edge over other biometrics companies in the pharmaceutical industry is the agile methodology we follow for clinical data management. Our seasoned data managers shorten timelines and help you get top quality data, leveraging innovative technologies.
Convert your ongoing as well as legacy data to standards specific to sponsors while adhering to CDISC standards. We can help you create datasets that are ready for submission, in real time. Additionally, our technology-backed data conversion and standardization approach helps to reduce submission timelines and facilitate smooth data analysis.
We can provide you scalable and flexible solutions that meet and exceed your biometrics functional needs. With our Functional Service Provider (FSP) model, you get a team of expert clinical data management professionals that serve as an extension of the sponsor. Boost scalability and quality while cutting down costs with our FSP model.
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