CDM is vital for clinical studies, involving the collection, management and cleaning of trial data to provide high-quality datasets for study analysis. Therefore data is being managed in the study database and quality control tools such as validation checks ensure that the data is discrepancy-free and complete.
Clinical data management not only handles high amounts of research data, but also ensures that the information collected in clinical trials is medically accurate, reliable, and compliant with regulatory standards. Key components of CDM are:
Database design and development: Designing databases tailored to specific clinical trial protocols, ensuring efficient data capture, storage and high quality of datasets.
Data governance: Establishing policies and standards for data collection, validation and cleaning.
Regulatory compliance: Ensuring all tools and data management practices are in compliance with legal and ethical standards, guidelines and regulations
At FGK, we reach these goals by cutting-edge clinical data management solutions tailored to the unique challenges of your clinical trial.
Experience the excellence of our data managers, your trusted partners in clinical data management. As the industry continues to evolve, the effective handling and utilization of clinical data become pivotal to accelerate innovation, enhance patient outcomes, and streamline regulatory processes.
… our State-of-the-art solutions
The rapidly advancing clinical research industry requires effective clinical data management tools to accelerate innovation, enhance patient outcomes, and streamline regulatory processes. Clinical research generates a wealth of data, from patient records and lab results to trial reports. The complexity and volume of this data can overwhelm traditional data management systems, hindering decision-making and slowing progress. FGK’s high-quality CDM solutions are designed to address these challenges head-on. They directly address these challenges, providing the users with information that enables smoother decision-making, faster progress, improved patient results and streamlined regulatory processes.
… our highly qualified and professional experts who think outside of the box
With a deep understanding of the pharmaceutical, biotechnology, and healthcare sectors, we are committed to facilitating your journey from data collection to actionable insights. FGK data managers record, compile and accurately pre-process your trial data. You can opt to have your data captured on paper and subsequently double-entered by our staff or electronically on site. Datasets are available in CDISC SDTM standard.
All employees in our Data Management department possess broad therapeutic expertise.
We offer eCRF solutions for sponsors, but our Data Management team can also work with any third-party EDC software on request.