Blog Flex Databases
e clinical trials are extraordinarily expensive and addendum to ICH GCP E6 R2 recommends to “encourage implementation of improved and more efficient approaches to clinical trial design, conduct, oversight, recording and reporting”, as well as to use risk-based approach when planning the activities in clinical trials, industry must move forward and utilize efficient procedures in any possible […]
10th Annual SCOPE Summit was held on 18 – 21 February in Orlando, Florida. If you have missed it for any reason, we are here to fill you in! Usually, all the insights we gather through an event are of two kinds: current industry problems and upcoming trends. This time we begin with Problems. Main […]
Good Clinical Practice is not only an industry standard – it is one of the core documents of our company, all of our modules are made in accordance with GCP. Interested? Request a demo via form on top of the page or drop us an e-mail to bd@flexdatabases.com
A few months ago, I left my three years’ marketing job in the automotive industry and started a new exciting journey at Flex Databases, eClinical software developer. Hard start in the clinical research world I knew that clinical research is complicated from my interviews and some research, so I decided to start learning during my […]
We’re excited to announce that we will begin our 2019 events with the upcoming 10th annual SCOPE Summit, 18 – 21 February in Orlando, Florida. As usual, we’re participating as exhibitors, so you can find us any day at booth #207! Evgenia Mikhalchuck, Director Business Development & Olga Sokolova, Director System Analysis will be happy to catch up […]
18th December 2018 EMA published a long-awaited “Guideline on the content, management and archiving on the clinical trial master file (paper and/or electronics)”. The release acquired many questions regarding the new reality of TMF, that everyone working in the EU will have to deal with after the document’s effective date 18/06/2019. How to make sure that […]
We are excited to announce our participation as exhibitors in the upcoming SCOPE Summit Europe, 16-17 October 2018 in Barcelona, Spain. Evgenia Mikhalchuk, Director Business Development, will be happy to catch up and show you the system. Step by our booth #4 to see our platform in action and learn more about Flex Databases! To plan a meeting drop […]
Flex Databases is always ready to support you in any challenging situation. And today, when GDPR came into effect, we are here to demonstrate that with us you are fully prepared to it in terms of our partnership. Here are some key GDPR requirements with explanation on how Flex Databases meet them: GDPR: Article 28.2 ‘The processor […]
We are excited to announce our participation in the upcoming 10th DIA China Annual Meeting, 23-25 May 2018 in Beijing, China. Meet with Olga Loginovskaya, MD, Chief Quality & Corporate Officer, and Timur Galimov, Chief Technology Officer, they will be happy to catch up and show you the system. To plan a meeting drop us […]
Clinical Trials are notoriously expensive to operate, with the majority of trial sites working with no more than a 3-month operating budget. That means that maintaining up-to-date financial records, and responsibly using what funds do exist is more essential than ever before. With an estimated two-thirds of trial sites falling into this category, software companies […]
The DIA 2018 Annual Meeting is one of the largest and longest running events in the life sciences industry. Step by our booth #1438 to see our platform in action and learn more about Flex Databases! To plan a meeting drop us a line at bd@flexdatabases.com
With so many CROs switching to an entirely digital format for their Trial Master Files, the legislators in charge of the regulations which govern compliance with international GCP standards are being forced to adapt as well. The nature of these changes has been conducive to simplifying and fortifying the entire auditing process, not only making […]