Clinical Trial Data Management Services
Our Clinical Trial Data Management solutions cater to biotech needs, ensuring precision from strategy to life cycle end. Strengthen regulatory submissions and fuel biotech innovations with our comprehensive controls.
Precision-Driven Data Management: Bolstering Biotech Breakthroughs.
At Celero, we prioritize precision and compliance in our Data Management Services. We are dedicated to preserving the integrity of your clinical trial data, aligning with key industry standards such as CDISC.
Understanding the crucial roles of tools like SAS and R in clinical trials, our collaboration is designed to provide top-tier Clinical Trial Data Management services. Through integrating SAS and R, we not only meet regulatory and industry standards but also empower unparalleled data analysis, propelling your clinical development projects to success.
Case Report Form Design
Entrust us with the intricate task of crafting case report forms (CRFs). Abiding by the gold-standard CDASH (Clinical Data Acquisition Standards Harmonization) guidelines, our seasoned data management team crafts CRFs that are not only lucid but fully compliant with regulatory directives.
Data Collection
Our Clinical Trial Data Management services are steeped in the CDISC ethos, particularly the SDTM (Study Data Tabulation Model) for regulatory submissions. Leveraging cutting-edge data collection technologies, we promise both punctuality and precision in data entry into the designated study databases.
Data Cleaning
Employing the ADaM (Analysis Data Model) standard, we embark on a rigorous data cleaning process. Harnessing sophisticated technologies, our experts pinpoint and rectify discrepancies, ensuring only top-tier data makes the cut.
Advanced Data Analysis
Delving deep into data, our adept managers employ statistical software powerhouses like SAS and R, all while staying faithful to CDISC standards. This commitment facilitates the creation of robust clinical study reports and regulatory dossiers. Our statistical methods uncover pivotal data trends, fortifying study objectives.
Global Coverage
Celero Executive team have experience in 80 trials across multiple clinical development phases (P1-P4) in more than 29 countries (US, EU, LATAM, APAC and Africa).
Introducing the Celero Way
A pathway to high-quality, cost-controlled, accelerated trials tailored to your needs.
Learn more about The Celero Way or speak to our Clinical Trial Data Management expert.
Speak to an Expert
Speak to an Expert
We are successfully ISO 9001 certified, which further underscores our commitment to meeting internationally recognized quality standards for quality, reliability, and excellence.