Clinical services for your trials and regulatory projects
Keena Life Sciences offers a full range of clinical services, from CRA staffing to regulatory submission. These services serve pharmaceutical companies, biotechs, medical device manufacturers and CROs seeking a subcontracting partner.
Our clinical services in detail
Each of these four areas addresses a specific operational need, identified with you before the assignment begins.
Clinical Research Associates
On-site and remote monitoring, data verification and site follow-up.
Learn more arrow_forwardClinical Project Management
Local and international coordination, from study start-up to close-out.
Learn more arrow_forwardRegulatory Submission
Filing with ethics committees, ANSM and relevant authorities, through to amendment follow-up.
Learn more arrow_forwardDedicated Support
Individualized support, for a targeted need on a specific phase or issue.
Learn more arrow_forwardA hybrid model, adapted to your organization
These clinical services combine according to your needs. You can request one-off reinforcement on a single position, or comprehensive support across several areas of the same study.
This modular approach suits sponsors structuring their first trial as well as CROs looking for a subcontracting partner.
A simple entry point for a complex need
You don't always need to know exactly which service fits your situation before contacting us. Describe your operational issue, and we'll direct you to the most suitable format, or a combination of several clinical services.
CRA reinforcement can, for example, come with ad hoc support in regulatory submission, when the study timeline requires it. Our teams then coordinate both areas under a single point of contact.
What sets our approach to clinical services apart
We don't offer a fixed catalog of standardized services. Every assignment starts with a scoping conversation, to understand your organization, your protocol and the constraints specific to your study.
This tailored approach applies equally to a few weeks of reinforcement and to structuring support spanning several years. It remains the same whether you're a pharmaceutical sponsor, a growth-stage biotech, or a CRO seeking a subcontracting partner.
For a one-off or recurring need, discuss your outsourcing needs with our team arrow_forwardEach of our clinical services relies on the same compliance requirements: ICH GCP, Good Clinical Practice, and strict adherence to our partners' internal procedures.