Discover our history
Keena Consulting was established in 2021, born from over ten years of expertise in clinical development across various therapeutic areas: oncology, neurology, nephrology, cardiology, ophthalmology, rare diseases, and medical devices. Founded after thorough reflection, the company emerged from the conviction that it was essential to mobilise experienced experts to support pharmaceutical laboratories, biotechnology companies, CROs, and medical device manufacturers in response to specific needs, whether they are short-term or long-term, to effectively manage their clinical trials.
Keena Consulting assists its clients in all critical stages of their studies: from start-up activities (selection of investigator sites, regulatory submissions, contract negotiations with institutions) to international project management, including site initiation, clinical trial monitoring, and site closure.
Keena Consulting stands out for its tailored approach, enabling its partners to navigate the challenges of clinical development with expertise, flexibility, and rigor.
Our services
Keena Consulting is an expert in project management support for the pharmaceutical sector, offering solutions tailored to the specific needs of businesses. We provide the development of customised materials, such as compliance documents and training tools, to ensure effective communication.
Our team is well-versed in pharmaceutical regulations, thereby ensuring compliance with current standards. Through our strategic approach, we assist our clients in optimising their processes and enhancing their performance.
Choosing Keena Consulting means securing a reliable partner to navigate the complex landscape of the pharmaceutical industry.
Our success stories
Keena Consulting has achieved numerous successes in conducting completed audit studies, thereby strengthening its reputation in the pharmaceutical sector. Our expertise in international regulatory compliance ensures that all our projects, including clinical trials, adhere to the highest standards.
Through our rigorous approach, we deliver reliable and high-quality results, contributing to innovation and the safety of treatments in the healthcare industry.
More than 20 supervised clinical trials
Excellence garantie
Partnership with 6 global industry leaders
Service optimal
Expertise in international regulatory compliance
Niveau supérieur
Management of more than 15 clinical studies and registries
Qualité vérifiée
100 % of audits successfully completed
Valeur réelle
Contact us
What if we met? Our Consulting Firm supports you in your project.
Certified experts, in-depth knowledge of the pharmaceutical sector for over 10 years
Contact us as soon as possible to develop your project!
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Our satisfied customers
At Keena Consulting, client satisfaction is at the heart of our mission, particularly thanks to our expertise in piloting clinical trials and managing supervised studies in oncology.
We ensure successful launch and efficient management of clinical trials, respecting pharmaceutical compliance and ethics standards.
Our commitment to carrying out each project with respect for confidentiality ensures our clients reliable and high-quality results in the healthcare sector.
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