Blog Flex Databases

Electronic Trial Master file (eTMF) – one of the must-have software solutions for a pharmaceutical company or a CRO nowadays. Almost any company either already has one implemented or thinking about it (and if you are – check out our how-to article on moving from paper to eTMF!) As everything, eTMF concept develops with time, moving […]

United States-based Tranquil Clinical Research recently signed Flex Databases as a software provider for Clinical Trial Management System and Pharmacovigilance management solution. Tranquil’s ultimate goal is excellence in the clinical trial process and bringing trustworthy products to patients. Flex Databases CTMS and Pharmacovigilance system are well-known as unified yet flexible eClinical platform for full-cycle clinical trial management. Baseline implementation takes […]

This June Assign Data Management and Biostatistics – Assign DMB chose Flex Databases as a provider for CTMS, eTMF, and Pharmacovigilance management systems. We’ve asked Dr. Anton Klingler, CEO Assign DMB and Mag. Sabine Haid, Lead Project Manager, a few questions about the upcoming partnership: Why Assign DMB decided to pick Flex Databases as a provider for […]

Investigators & Sites Management – Flex Databases CTMS module.  Investigators & Sites Management Module helps to organize all information on investigators, sites, vendors, therapeutic areas, IRB/LECs, etc. It provides easy search capability for feasibility assessments and other needs. Video duration: 06:25

Sourcia, a full-service European CRO, has recently signed a contract for electronic Trial Master File implementation with Flex Databases. We’ve asked Claudia Gruber, Director Clinical Operations a couple of questions about the upcoming partnership: Why has Sourcia decided to pick Flex Databases as an eTMF provider? CG: To foster and allow for our continued growth, […]

Today is the day, dedicated to all of us who work in clinical trials – International Clinical Trials Day. Even though we are parted physically, for now, we are all together grateful for being a part of the industry. We praise the braveness and tirelessness of everyone, who is investing their precious time into finding […]

One of the main factors stopping companies from moving to an eTMF is the actual moving process. When you think about transferring a ton of documents from paper to electronic, it usually seems to be just an impossible work. With Flex Databases eTMF all you need to move from paper to electronic Trial Master File is three […]

When we ask our clients why they’ve decided to implement one or another system, among many reasons, we always have something budget-related – it might be financial transparency, cost-effectiveness, and other variations. Financial transparency is a big subject that we will cover soon in a separate article, but today is for cost-effectiveness. Four ways how Flex […]

Over a month ago, we at Flex Databases moved our employees to work from home due to a pandemic outbreak. We have met challenges, part of which are solved, and some are still ongoing. The situation is going to develop further, but the time has come to take a deep breath and review where we […]

Trial Master File 6.0 Learning Management System 4.2 Subject Tracking & Invoicing 4.0 CRA Activity Management 2.1 Investigators & Sites Management 3.1 Quality Management System 1.0 Quality Management System is based on workflows from the Workflow Management module. Expense Reporting 2.0 Request a demo or send us an e-mail to bd@flexdatabases.com to know more!

Electronic Trial Master File or eTMF is not a new thing on the market, yet there are still companies working with paper solutions. Of course, every single eTMF provider now has a “Now it’s time to change to eTMF because it’s online” kind of article, but we at Flex Databases believe, that eTMF is more than just […]

Yesterday morning FDA has released the Guidance on Conduct of Clinical Trials of Medical Products during the COVID-19 pandemic. Here are the parts of Guideline recommendations that may be successfully followed with Flex Databases system: Protocol deviations and IRBs/IEC submissions tracking The Guideline states, that “FDA recognizes that protocol modifications may be required and that there may […]