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March 2020

Banook Group welcomes Turenne Santé as new investor, alongside the management

Funds obtained will enable the European leader in cardiac safety to continue its…
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May 2018

Webinar : Advances in cardiovascular diagnostic devices for clinical trial

Tuesday, May 29th, 2018  6:00 PM CEST (Central European Time) UTC/GMT + 2…
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April 2017

Event Participation 2017

Banook Group will attend the following exhibitions. Let’s meet there!
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February 2017

Cardiabase by Banook Group opens subsidiary in Montreal, Canada

Group strengthens its presence in North American market, aiming for 30% growth in…
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March 2015

Banook Group - New branding announcement

Cardiabase/Banook Central Imaging becomes Banook Group - New branding announcement.
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March 2014

Webinar: Imaging anti-cancer treatment response at a preclinical and clinical stage

Use of imaging in oncology clinical trials is mainly based on morphological evaluation…
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Mission & strategy > Our strategy > Constantly enhancing our responsiveness and proximity

Our strategy

Relying on talented women and men
Constantly enhancing our responsiveness and proximity
Implementing an optimal quality system
Developing partnerships



Banook Group can provide rapid and easy access to top-flight experts, whose scientific and regulatory expertise encompasses a broad range of clinical and regulatory issues. Indeed we can offer scientific, operational and technological solutions rapidly, even for complex trials.





Rapid availability of our scientific and technical experts, along with our time saving operating procedures, help you expedite the conduct of your clinical trials. Our teams monitor project progress closely to detect any scientific or operational issues that could delay your program. When this happens, our experts are alerted, rapidly review the issue and communicate with you to propose solutions that keep your project on track or even shorten its execution. Furthermore we provide final data reviews in a short time frame enabling you to lock databases and file marketing applications faster.


Our ability to being responsive and proactive in a balanced way are an assurance of data quality and time and cost savings while maintaining the safety and integrity of your clinical trials.



Our teams and experts are able to:


  • rapidly respond to issue and routine calls,
  • rapidly provide scientific expertise,
  • rapidly adjust to specific protocol requirements,
  • rapidly mobilize “within the scope reviewers”,
  • rapidly deploy an operational team for setting up a new project,
  • rapidly address issues during study conduct, and
  • provide the agreed-upon deliverables in a short-time frame.