We are proud to announce our participation in the upcoming PHUSE EU Connect 2024, taking place in Strasbourg from November 10-13. Read more about our PHUSE journey over the past years in the article.

When launching a clinical trial, the quality and integrity of your clinical data management are paramount. Choosing the right Contract Research Organization (CRO) to handle CDM services is crucial to ensuring the success of your study. Our team at STATECS highlighted some key factors you should consider when selecting a CRO for your CDM needs.

Clinical Data Management (CDM) is crucial for clinical research for gathering trustworthy, high-quality, and statistically sound data. The CDM process begins with the tip in mind. As a trial is intended to answer the research question, the CDM process is intended to deliver an error-free, valid, and statistically sound database. To satisfy this objective, the CDM process starts early, even before the finalization of the study protocol.

The purpose of Clinical data management (CDM) is to handle the data that results from clinical trials which all aspects of processing study data are a part. To support the gathering, cleaning, and management of subject or trial data, including designing and maintaining software systems, and databases by following necessary procedures and protocols.

Clinical trials play a pivotal role in ensuring the safety and efficacy of new medical interventions, treatments, and therapies. As the complexity of clinical trials continues to grow, so does the need for sophisticated tools and technologies to manage, analyze, and interpret the vast amount of data generated.

SAS (Statistical Analysis Software) is a widely used software suite for data analysis and visualization. It was first developed in the 1970s and has since grown into a comprehensive tool for advanced analytics, business intelligence, predictive analysis, and data management.