Streamline data between BSI CTMS and the EDC solutions from our partners

BSI is working with various Electronic Data Capture (EDC) partners to deliver a complete eClinical platform.

Greenlight Guru

Greenlight Guru Clinical (formerly SMART-TRIAL) is the leading clinical data collection toolbox, purposefully built for MedTech. Collect and manage clinical data in pre and post-market clinical studies, including registries, cohorts, surveys, human factor testing, design validation, and more. Greenlight Guru Clinical meets the regulatory requirements of the FDA, EU, and most other countries, and ensures compliance out-of-the-box with GCP and ISO 14155:2020.

Learn more about Greenlight Guru Clinical.

Marvin

Marvin EDC is a secure, cloud-based Electronic Data Capture software designed to manage clinical trial data, particularly for complex and oncology studies. It facilitates study setup, data collection, and monitoring, supporting FDA/EMA compliance. Key features include RBM (Risk-Based Monitoring), ePRO, eConsent and randomized trial management.

Key Aspects of Marvin EDC:

Core Functionality

Enables secure, browser-based data entry
(including double data entry)
Data validation
Real-time monitoring of clinical trial sites
Powerful Amendments with no downtime

Extended Capabilities

Highly suited for complex trials in e.g. oncology due to its flexibility in handling complex workflows.

Goes beyond basic EDC with features including:

AI-powered Study Setup
Randomization (IWRS/RTSM)
Enhanced Safety Workflows (AI Case Intake)
ePRO
Local and Central Lab Module
Risk-based Monitoring
Medical Coding

Compliance & Data Quality

CDISC ODM-certified
Complies with 21 CFR Part 11
Complies with ICH-GCP standards

Marvin EDC is widely used by researchers to ensure accurate data capture and streamline the data management process. Developed in Germany by AB Cube Germany, Marvin EDC has supported over 1,500 studies worldwide since 2002

Learn more about Marvin.

Viedoc

Viedoc Technologies designs engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster. We accomplish this by combining technology and creative design to streamline, automate, and simplify conventional processes within clinical research. Founded in 2003, Viedoc Technologies has become a leader in Electronic Data Capture (EDC), offering full support for decentralized clinical trials, unrivaled setup times, high-level security measures, and global support.

Learn more about Viedoc

Zelta by Merative

Zelta™ by Merative is a clinical trials solution business that includes both a clinical data management and acquisition platform and consulting, enablement, and extension services. Zelta’s unified cloud-hosted platform supports all phases and complexities of research, including over 450 phase III trials.

Maximize patient, caregiver, and provider engagement by choosing only what you need from these fully integrated modules:

Clinical Data Management & Acquisition