Data Conversion and Standardization
Technology driven data conversion and standardization services help you shorten submission timelines, streamline data analysis, and facilitate real-time creation of submission-ready datasets
Clinical Data Standardization and Conversion, Simplified
The eCS data standardization team supports conversion of both ongoing and legacy data to sponsor-specific standards in compliance with CDISC standards for clinical trials. Starting with data collection using CDASH to submission using SDTM and analysis using ADaM, access any level of assistance for your clinical data conversion and standardization needs.
Unlock the value of your clinical data
The eCS data services team supports your CDISC standards clinical data management efforts by ensuring your data is not only submission-ready, but can be utilized efficiently for data exploration and analysis based on your specific needs. Available clinical data standardization and conversion services include:
- SDTM and ADaM mapping, programming and validation services
- SDTM-annotated CRFs compliant with CDISC standards for clinical trials and FDA requirements
- SDTM and ADaM Reviewer’s Guides accompanying submissions
Quality data to further your development process
The eCS data conversion and standardization team combines their thorough understanding of clinical data workflow requirements with innovative technology such as eClinical’s elluminate Mapper to provide you efficient data mapping while adhering to strict standards of quality. Gain expert assistance with:
- Mapping of clinical data to repositories and into structures aligned to submission requirements
- Building of standard programming and metadata libraries, for mapping reusability
- Ensuring QA compliance of mapped data against submission requirements
Frequently Asked Questions
What are Technology Enabled Clinical Data Services?
eClinical Solutions data services teams accelerate your timelines and help you produce the highest quality data through expert use of technologies including the eClinical Solutions core platform, the elluminate® Clinical Data Hub, and Medidata’s Rave Clinical CloudTM.
What type of Biostatistics and Statistical Programming Services do you offer?
eClinical Solutions biostatisticians and statistical programmers lead the way for all of your statistical needs, from authoring the Statistical Analysis Plan and preparing your Tables, Listings and Figures to providing ADaM deliverables and ISS/ISE submission packages. Services include developing mapping methodologies, organizing content into a structure aligned to submission requirements, and facilitating incorporation into the submission, mapping data into clinical data repositories. eCS statistical programmers bring CDISC standards expertise and in-depth knowledge and experience in producing FDA compliant datasets and TLFs towards submission. Generate SDTM-annotated CRFs compliant with CDISC guidance and FDA requirements, as well as SDTM and ADaM Reviewer’s Guides accompanying submissions.
What is the benefit of working with a data-focused Services Provider vs. a full service CRO?
Our philosophy and model is for sponsors to identify the best in breed CROs to meet the specific needs of each trial. Data management should be the consistent cornerstone of the development program to ensure efficiencies are realized (both time and money) from trial to trial. Our entire focus is on sponsor data with our mission to make clinical data acquisition and analysis easy and intelligent to help bring new treatments to patients faster. This focus and commitment to your clinical data allows us to be efficient, have proven expertise and provide a consultative approach to ensure your data meets your development requirements.
What benefits does elluminate provide for Data Services clients?
elluminate is utilized in all data services projects to provide advantages such as data integration and centralized access, standardization using elluminate Mapper, and real-time data review and visualization with Data Central and Clinical Analytics. elluminate gives both our clients and Data Managers complete transparency into the data during trial conduct and beyond, without the need for time-consuming and costly programming. You and your eCS data services team are empowered to make quicker critical decisions with powerful visualization and advanced analytical intelligence for all your clinical data from any source, in a standardized format.
What therapeutic areas do you have experience in?
eClinical Solutions is experienced in many therapeutic areas including Cardiovascular, Endocrine and Metabolic, Gastroenterology, Hematology & Oncology, Immunology, Infectious Diseases, Rare Disease, Respiratory, Urology and Vaccine. eCS project teams have extensive experience conducting complex trials such as oncology, rare disease and gene therapy.
Do you only do study builds using the Rave Clinical Cloud?
eClinical Solutions was one of Medidata’s first accredited partners to support Rave, achieving Services accreditation in 2008 and Technology accreditation in 2012. eClinical Solutions is the only Medidata partner to commit to their platform, in that we will only perform Rave study builds. eCS could support data management activities leveraging other EDC systems, but we believe in having the deep expertise and experience needed to master study database configuration.
What is unique about your relationship with Medidata?
Sponsors working with Medidata & eCS experience increased control over their clinical data through access to all trial data including legacy Rave studies across CROs and sources via elluminate. A real-time, tightly coupled integration between Rave & elluminate provides visibility, oversight, cost savings and control. eCS is the only Data Services provider that is dedicated to the Medidata Rave platform with 9+ Medidata certifications and 11+ years of partnership. You also gain maximum reuse of optimized data collection designs, standards and libraries through URL management/ownership for sponsors.