At SBR Clinical Research, we offer you a custom-designed clinical trial package
which is affordable to your budget. Thoroughly developed by our experienced team, we create all trial documentations including the protocol, informed consent form, participant information leaflet, and the electronic database; as well as the submission to relevant regulatory bodies for ethical approvals.
We also present a growing pool of participants eager to get involved in research.
You can be rest assured that the SBR Team will manage the entire campaign of
recruiting and coordinating the trial participants, in accordance to the protocol.
In addition to this, SBR provides independent data quality monitoring throughout
the trial, to ensure the continued relevance and credibility of the clinical data, as
well as the maintenance of any amendments that may need to take place during the
At the end of the trial, you will be provided with a rich set of statistically analysed
data, to present your product’s safety and efficacy in the best way possible. We can
even help you with additional services, such as the appropriate presentation of your
data on your marketing platforms, and prospective further product development.
We aim to give you a hands-off experience in conducting a clinical trial, but will
always maintain transparent communication with you throughout the process, with
a view to making the clinical trial experience as easy and as rewarding as it needs