AB Cube | Life Sciences Trusted Cloud Software
Our Global Partners in Safety & Innovation
AB Cube partners with global leaders to enhance pharmacovigilance, streamline data exchange, and expand the SafetyEasy® Suite’s reach for safer, smarter healthcare.
A Decade of Collaboration in Pharmacovigilance Excellence
With nearly 35 years of experience, Biotrial stands as a trusted and innovative Contract Research Organization (CRO), offering a comprehensive suite of services that span the entire drug development lifecycle. Our long-standing collaboration reflects a shared commitment to advancing clinical research and delivering high-quality, patient-centric solutions.
Biotrial’s Core Services Include:
- Preclinical Pharmacology: Expertise in early-stage drug evaluation, including discovery, safety, efficacy, and pharmacokinetics studies.
- Clinical Development: Phase I studies with healthy volunteers and special populations, as well as patient-based trials across many different therapeutic areas.
- Biometrics & Data Science: Robust data management, biostatistics, and advanced analytics to support regulatory submissions and strategic decision-making and explore beyond the boundaries of traditional clinical trials.
- Bioanalysis: High-quality LC-MS/MS bioanalytical services for drug quantification in small and large molecules and biomarker analysis.
- ECG, EEG CNS & Imaging Core Lab: Specialized capabilities in central nervous system studies, cardiac safety testing and advanced imaging techniques.
- Tailor-Made Solutions: Flexible, scalable approaches designed to meet the unique needs of biotech and pharmaceutical sponsors.
- Global Reach: Clinical Pharmacology Units in the USA and France, laboratories in France and Canada, offices in the UK, enabling international trial execution with local expertise.
Together, AB Cube and Biotrial offer a powerful combination of technology-driven pharmacovigilance and clinical research excellence — supporting sponsors from early development through post-marketing surveillance.
AB Cube and EXTEDO: Expanding Global Reach Through Strategic Reselling
EXTEDO is a leading provider of life sciences information management software and services for industry and health authorities worldwide. As a reseller of AB Cube’s SafetyEasy® Suite, EXTEDO helps extend the reach of our pharmacovigilance technology to regulatory and safety teams across the globe.
By offering their customers access to SafetyEasy’s cloud-based, E2B (R3)-compliant safety solution, EXTEDO enhances its comprehensive solution EXTEDOpulse, enabling efficient and compliant adverse event reporting and safety case management, thus guaranteeing Effortless Compliance throughout every step of drug development.
This collaboration supports:
- Broader market access to SafetyEasy® Suite
- Streamlined pharmacovigilance workflows for EXTEDO clients
- Regulatory-ready solutions aligned with global standards
Together, we empower life sciences organizations to manage safety data with greater efficiency, compliance, and confidence.
Enhancing Collaboration Between Clinical and Safety Teams
As part of our commitment to seamless pharmacovigilance, AB Cube and Marvin have partnered to integrate the Marvin EDC systems with the SafetyEasy® Suite.
This integration enables a direct, automated flow of safety cases from Marvin to SafetyEasy®, significantly improving collaboration between clinical investigators and safety teams. The result?
- Earlier signal detection
- Faster case processing
- Improved patient safety outcomes
By bridging clinical and safety data environments, this partnership supports a more proactive approach to pharmacovigilance, especially in complex, multi-site studies.
And this is just the beginning—more updates are coming in early 2026 to further enhance this integration.
Learn more about the benefits of our systems integration here: https://xclinical.com/clinical-data-management/
Integrating Safety and Clinical Data for French Hospitals
Telemedicine Technologies is a leading provider of eHealth solutions for clinical research, known for its secure and modular platform CleanWeb™. Through our collaboration, SafetyEasy® has been successfully integrated with CleanWeb™ to support clinical trials and pharmacovigilance operations in French hospitals.
This integration enables a direct and automated flow of safety data from clinical trial systems to SafetyEasy®, improving the speed and accuracy of adverse event reporting and signal detection.
Key benefits of this partnership include:
- Streamlined data exchange between EDC and safety systems
- Improved collaboration between clinical and safety teams
- Earlier signal detection and faster case processing
- Support for French hospital networks conducting clinical research
Together, we’re enhancing the safety infrastructure of clinical trials in France, ensuring better outcomes for patients and more efficient workflows for investigators.
Supporting QA and Validation and Regional Expertise in APAC
Valina Services plays a key role in supporting AB Cube’s SafetyEasy® Suite through expert QA and validation services and regional collaboration across the Asia-Pacific (APAC) region.
With deep knowledge of Computerized System Validation regulatory requirements and standards ( GAMP5®, FDA CFR21 Part 11, …), Valina Services helps ensure that SafetyEasy® Suite deployments meet the highest regulatory and technical requirements.
Their support enables AB CUBE to provide pre-validated software, and our clients to benefit from up-to-date validation dossiers, automated system updates, and minimal additional validation effort.
In addition, Valina’s presence in APAC strengthens our ability to deliver localized support, training, and implementation services, ensuring smooth onboarding and compliance for regional clients.
This partnership brings:
- Expert QA and Validation support for regulatory readiness
- Localized services for APAC-based clients
- Streamlined deployment of SafetyEasy®Suite solutions
- Enhanced global reach and responsiveness