How CRA Activity Management impacts daily life of a CRA

March 17, 2020

How CRA Activity Management impacts daily life of a CRA

If we imagine clinical trials as a human body, Clinical Research Associates would be the blood cells. They travel a lot across the whole organism, delivering data oxygen to all organs and body parts. If something stops the proper functioning, it may result in global failure. That’s the reason why we developed CRA Activity Management module – to help our clients ensure and support the proper CRA’s functioning. 

From hours to minutes

Optimization starts with routine tasks. It usually seems like routine is effortless and not time-consuming, but it might take away the most significant part of the day. 

With Flex Databases CRA Activity Management you’ll get:

  • Customizable widgets on the first screen: simple tracking of the most critical metrics of user’s choice. 
  • All Monitoring Activities stored in one place: instead of checking multiple task managers, CRA can follow one, with tasks lined up by deadline (upcoming visits are included). 
  • Simple site visit planning and scheduling: centralized calendar to oversee workload and plan visits accordingly. 
  • Customizable templates for confirmation and follow-up letters: push a button in the system and get your letters done in 1 second, the system will take care of the rest. 
  • Simple contact report creation. 
  • All documents are filed into TMF automatically and immediately after completion. 

By organizing the routine, Flex Databases CRA Activity Management helps to reduce the amount of time spent on it from hours to minutes or even seconds, if we talk about fully automated features such as TMF filing. 

Reporting made easy

CRAs manage multiple sites at once, and with such workload, it’s easy to get lost and fill in a wrong report. The system helps to maintain and decrease the number of errors caused by the human factor by organizing information clearly and simply. 

  • The system picks the type of visit report according to the type of the visit: PSV, SIV, IMV, COV.
  • Automated notifications remind about reports that must be written, completed or passed the review to keep the user aware of the actions that need to be done in the future.
  • Offline reporting possibility is aimed to help road warriors keep on going even when the connection is poor or non-existent (on a plane, for example). 
  • All required fields are marked, and it’s impossible to submit an incomplete report. 
  • Inbuilt problem control: action items, protocol deviations tool keeps track of all the issues, occurred with sites. 
  • Ad-hoc reporting tool for cross-project and cross-module reporting (graphs, widgets) – all the data the user might need is on the table in a simple click. 

CRA’s life is not the simplest one, but it surely can be more comfortable with CRA Activity Management.

To know more, request a free demo via button on top of the page or send us an e-mail to bd@flexdatabases.com.

Blog

December 19, 2024
Product Updates: December, 2024

We are excited to announce several new features and improvements to Flex Databases’ modules. These updates aim to streamline workflows, enhance usability, and improve overall efficiency for our users. Here’s an overview of the latest developments and their benefits. Trial Master File (TMF) Duplicates Search: Files Content Comparison Path: Trial Master File → (open project) […]

December 18, 2024
How Clinical Trial Sites Can Meet Sponsor Expectations in 2025

Clinical trials are becoming more complex every year, and sponsors are raising the bar for what they expect from sites. They want faster processes, more accurate data, and better ways to keep patients engaged – all while staying compliant with ever-evolving regulations. As we look ahead to 2025, these demands will only grow. New technologies […]

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 […]

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.