Clinical Data Management (CDM)

BioData Partners evaluates your study requirements and selects appropriate methods to ensure data integrity, precision, and quality at every step of the process. Our comprehensive CDM guides encompass critical capture, collection, and retention strategies that are essential to clinical trials.

Expertise

Quality

Delivery

eClinical Solutions

Our eClinical solutions are designed to help sponsors manage the vast amounts of data generated during a trial, as well as improve the efficiency and accuracy of various tasks such as data collection and reporting.

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Looking to implement a reliable electronic data capture (EDC) solution for your clinical trial?

Our team is available to provide exceptional support and guidance, ensuring that you get the most out of the EDC platform you choose.

Need a reliable EDC solution without the cost of implementation?

We have partnerships with multiple EDC vendors. Our preferred platform is designed to streamline your data collection and management processes, so you can focus on what matters most—advancing your research.

Configure your casebooks for master protocols and adaptive trials with less time and effort. Make mid-study amendments with zero downtime and no migrations. It is modern, agile, and fast—dramatically improving the user experience for sites, monitors, and data managers.

Is external data keeping you up at night?

We have a team of experts who can guide you through the challenges of managing diverse data sources and data reconciliation. With our specialized knowledge and experience, we can help you navigate the complexities of these processes. Let us support you in streamlining your data handling procedures, so you can focus on what you do best—driving your clinical trial forward.

Our CDM Services

Data Management Plan (DMP)

Outline scope, process, and methods of clinical data management for study stakeholders.

Data Validation Plan (DVP)

Define DMP-based guidelines to resolve trial data discrepancies and inconsistencies.

Database Design

Design fit-for-purpose study database to accurately record all multi-source clinical data.

Medical Coding

Translate patient data into standardized medical code that is easy to interpret.

Database Locking

Secure database and define authorized users, audit plan, and revocation procedures.

External Data

Streamline data handling procedures to move your clinical trial forward.

Need help selecting the right technology for your trial?

BioData Partners integrates EDC, RTSM, and ePRO data management tools to fit your requirements.