Flex Databases recognised as one of top-10 Pharmacovigilance providers in the UK & Europe

October 5, 2022

Flex Databases recognised as one of top-10 Pharmacovigilance providers in the UK & Europe

This September, Pharma Tech Outlook included Flex Databases in Top-10 Pharmacovigilance solutions providers in the UK & Europe.

Our Business Development & Marketing Director Evgenia Mikhalchuk took part in a cover story for Pharma Tech Outlook September’22 issue, supporting our nomination:

Clinical trials have always been about data. But, prior to automation, data input was a major concern.
For us, it is crucial to concentrate on whether the data is actually functional for everyone while also ensuring that its consumption is as simple as breathing.

The company’s software solution is based on materialising this expression and providing a system for clinical trials that is automated, uncomplicated, and ensures compliant pharmacovigilance activities throughout all the trial stages. A highly comprehensive, flexible, and intuitive solution, the tool enables its users to meet the rapidly evolving requirements of clinical investigation, catalysing the trials’ progress swiftly.

To perform multi-fold tasks, including data collection and assessments in clinical trials, Flex Databases facilitates a BI (Business Intelligence) reporting tool that is designed to provide instant data accessibility for further interpretations and actions. The tool eliminates labor-intensive, repetitive data inputs required in performing critical undertakings such as planning and reporting. Additionally, it empowers clinical research enterprises with insights to gain increased visibility into study progress. 

Our software solution is based on materialising this expression and providing a system for clinical trials that is automated, uncomplicated, and ensures compliant pharmacovigilance activities throughout all the trial stages. A highly comprehensive, flexible, and intuitive solution, the tool enables its users to meet the rapidly evolving requirements of clinical investigation, catalysing the trials’ progress swiftly. 

The company’s software solution is based on materializing this expression and providing a system for clinical trials that is automated, uncomplicated, and ensures compliant pharmacovigilance activities throughout all the trial stages. A highly comprehensive, flexible, and intuitive solution, the tool enables its users to meet the rapidly evolving requirements of clinical investigation, catalyzing the trials’ progress swiftly. 

The company stands out distinctively in its approach to handling its clients’ clinical data management concerns earnestly, facilitating a transparent collaboration with them. It helped one of its clients in the research of COVID vaccines during the compelling times of the pandemic. The research required the integration of several data sets into Flex’s architecture while maintaining the system’s performance for search, analysis, and signal detection. Interestingly, during the course of this engagement, Flex Databases successfully aggregated hundreds of thousands of cases within its analysis system without hampering the efficiency of results obtained. The company demonstrated exception resilience and readiness through its solutions, especially during the testing times of the pandemic. 

To read the full interview and explore Flex Databases profile, you can either do

Blog

December 2, 2024
Flex Databases Achieves ISO 27001 Certification

We’re pleased to announce that Flex Databases’ IT security measures are now formally certified under ISO 27001. This certification, earned after a thorough audit, demonstrates that our systems meet internationally recognized standards for information security. ISO 27001 sets requirements for managing sensitive company and customer data securely. By achieving this milestone, we assure our clients […]

November 28, 2024
The Future of AI in TMF

The Trial Master File (TMF) is the cornerstone of clinical trial documentation, serving as the definitive record of compliance with regulatory standards and ethical guidelines. Yet, the management of TMFs has grown increasingly complex with the rise in document volume, diversity, and stringent compliance requirements. Artificial intelligence (AI) is poised to address these challenges, introducing […]

November 19, 2024
How to Choose Pharmacovigilance (PV) Software for Clinical Trial Management

Pharmacovigilance (PV) is a critical aspect of drug safety, focusing on detecting, assessing, understanding, and preventing adverse drug reactions or other drug-related problems. As global regulatory requirements for drug safety evolve, adopting reliable pharmacovigilance software has become essential for ensuring compliance and improving operational efficiency. Selecting the right PV software can significantly impact your organization’s […]

November 14, 2024
How to Integrate CTMS with EDC

Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems are critical to the effective management of clinical trials. By integrating CTMS and EDC, organizations can streamline processes, enhance data quality, and improve overall efficiency. Here are five key tips to ensure a successful CTMS and EDC integration. Effortless Integration of Flex Databases CTMS […]

Contact us

Get in touch to discuss compliance, implementation, demos, pricing

We are here for all of your questions! Tell us more about yourself and we will organize a tailored live demo to show how you can power up your clinical trials processes with Flex Databases.