When we build a product, we base its core on the challenges our customers may face and how to solve them. We step in your shoes to see things from your point of view – what you need. Here’s the list of challenges that you have, and we solve – and how exactly we solve […]
As we briefly discussed in the previous chapter, Artificial Intelligence (AI) is used to simulate the processes of a human brain with the help of computer systems. It encompasses various technologies, including rule-following, reasoning – using rules to reach rough or specific conclusions, learning, and self-correction. Implementation areas of AI In the area of pharmacovigilance […]
Modern pharmacovigilance, like any other process, in 2021 is impossible without technology and automation. The presence of an electronic system is a guarantee of high-quality and fast collection and processing of safety data. But even with an electronic system in place, it’s not possible to 100% avoid manual labor of collecting and entering data. But […]
So, here’s the deal: with any data point in our system, you can make a report and visualize your data. And it’s free. And it takes just a few clicks to create. How it works: Step 1: Select data sources 2. Provide permissions You can share your custom reports with anyone you like, from your […]
Clinical Trial Management System (CTMS) Manage all your CRA activities, patients’ data, sites, and invoicing in real time. Project Management & Budgeting Make the complex financial part of your project easy Electronic Trial Master File Gain complete visibility into all of your trial documentation Pharmacovigilance Ensure robust and compliant pharmacovigilance activities throughout all the trial […]
There are many factors to consider when purchasing a clinical trial management software – from regulatory requirements to the sponsor’s wishes. Many of these factors could be summarized to a need. To comply with the need, you create a checklist with major and minor features and flows to implement. But, keeping in mind that every business is […]
It all started with a big bang small team of professionals aiming to build a masterpiece of a product and a company. Now we are almost a hundred, and it couldn’t have been better. 2011: From 5…. 2021: …to 70 and counting Vlad K, Product Director Karine D, Project Manager During my first year at Flex Databases, […]
This summer ABX-CRO and Flex Databases signed a contract for a CTMS & eTMF implementation. We asked Dr. Ulrike Schorr-Neufing, Director, Qualification & Training, ABX-CRO, a couple of questions about the upcoming partnership. Why ABX-CRO decided to pick Flex Databases as a provider? After an intensive selection and evaluation process comparing different service providers ABX-CRO […]
Even though electronic Trial Master File seems to be almost essential nowadays, there are still many questions on its value and benefits that it could bring to a company. We’ve decided to answer the most common and most important of them and walk you through the entire process – from Why select eTMF through Legacy data migration to Smart eTMF, which works […]
Recently, we discussed questions that might arise when changing your eClinical software provider. Today, we want to take a closer look at one of the most asked questions: How can I migrate data from a legacy CTMS or eTMF? Data migration is a delicate process with many moving parts. Without a well-established process, the CTMS go-live could […]
At the very beginning of 2021 Flex Databases and German FGK CRO signed a contract for CTMS and eTMF implementation. About FGK FGK CRO is a full service contract research organization offering a complete range of clinical development and consulting services to pharmaceutical, biotechnology and medical device companies. FGK approaches each project, whether large or small, with dedicated, highly motivated, small […]
Software validation is tricky, especially for those who’s never met it before. Still, it Is required, and it can affect implementation timelines in the worst way if handled poorly. That’s why we at Flex Databases developed a simple workflow to make validation almost effortless and as simple as possible: Step 1: We provide the happy new […]
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