Welcome to SBR Clinical Research
Have you created a unique product? Are you in the process of
developing a brand-new product? Or would you like to give
your existing product a competitive market advantage, with
research-backed claims?
If you answered YES to any of these questions, then you have come to the right
place! We are always on the lookout for exciting opportunities to collaborate with
brilliant companies like yours.
Who We Are
SBR Clinical Research is a London-based contract research organisation specialising in clinical trial design, participant recruitment, study coordination, independent monitoring, and statistical data analysis.
We have almost a decade’s worth of experience in the development and management of clinical trials, and can offer you a range of services from start (set-up) to finish (close-out); resulting in genuine and statistically credible data to verify the efficacy and safety of your products.
Conducting a clinical trial will give your product a highly desired edge in the market, allowing you to make honest, clinically-proven claims, which will give your consumers the added confidence to purchase from your company, and this in turn will drive your business growth!
What We Do
Clinical trials need not be complicated. We at SBR offer our clients a “hassle-free but always fully informed” service, so you can focus on what you do best, while we work hard to bring you those all important research-backed results.
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
trial.
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
to be.
Take a look at how we design, coordinate, and manage the process for you:
Trial Design & Set-Up
- Protocol Development
- Study Materials Development
- Regulatory Applications
Participant Recruitment
- Subject Pools
- Participant Retention
- Compliance Monitoring
- End of Study Follow-Up
Database & Monitoring
- Database Development
- Data Monitoring
- Safety Monitoring
Outcomes & Analysis
- Statistical Analysis
- Final Reports
- Further Research
- Marketing Strategies
Get In Touch With Us
Please get in touch with us to have a more in-depth discussion about the bespoke services we can offer, to meet your needs. We look forward to working with you.
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