Tranquil Clinical Research selects Flex Databases CTMS and Pharmacovigilance

July 27, 2020

Tranquil Clinical Research selects Flex Databases CTMS and Pharmacovigilance

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.

  • It helps to optimize and automate the most important aspects of any clinical trial process – monitoring, grants & subjects, and sites
  • It provides easy capability for financial management, study monitoring, feasibility assessments, and other needs
  • It is a secure and validated PV system that serves as a single point of entry, assessment, and reporting of safety data

Baseline implementation takes only 5 weeks!

Tranquil clinical research was created to ensure that the entire clinical trial, device, and drug development process is conducted with ethics and the patient in mind first and always. The business model ensures a client’s drug, device or investigational product in the clinical trial is adherent to the highest level of quality and integrity in the services company provides.

Blog

September 29, 2026
EDC Data Solution Specialist (Data Manager)

As an EDC Data Solution Specialist (Data Manager), you will work at the intersection of data, systems, and clinical research. You will translate clinical study requirements into practical EDC solutions – from understanding study protocols to building and testing electronic forms, configuring validation rules, and supporting clinical data throughout the study lifecycle. We are looking […]

September 24, 2026
How ITS Achieved 98% TMF Completeness and Cut Audit Prep Time in Half

About Integrated Therapeutic Solutions Integrated Therapeutic Solutions (ITS) is a clinical research organization (CRO) specializing in multi-country clinical trials. As ITS expanded its sponsor portfolio and study volumes, it demanded a document management infrastructure capable of keeping pace – one that could ensure regulatory compliance, support sponsor oversight, and maintain operational control across a growing […]

September 14, 2026
Flex Databases Product Updates: EDC, IWRS & eCRF Builder Updates That Remove Manual Work From Study Teams

Every month, Flex Databases ships updates driven by real friction our clients run into on active studies. July’s release focuses on one theme in particular: removing manual, repetitive work that takes up study teams’ time and creates avoidable errors. From protecting critical configurations to automating bulk data entry and site-specific workflows, these updates address everyday […]

September 8, 2026
Flex Databases Builds Your eCRFs In-House – So Your Study Doesn’t Have to Fit Someone Else’s EDC

How Flex Databases gives Sponsors more flexibility without compromising compliance by building eCRFs from scratch, in-house, for every client. Let’s face the facts: not every EDC provider actually builds the technology behind the study. When it comes to the eCRFs, many rely on third-party solutions. And while they still position their EDC as the best […]

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.