We are a bespoke, clinician led, clinical trials support service, meeting the needs of organisations trialling their products and devices in healthcare settings.

We specialise in Med Tech innovations, and have particular experience in Med Tech destined for primary care and community settings whilst working in partnership with secondary care.  We are uniquely placed in this field, offering clinical staff to lead on protocol writing, MHRA applications, as well as providing a CQC registered in-house mobile nursing service for hybrid trial delivery that crosses over from secondary care to community settings, and from NHS into private.  Every project we engage with is overseen by a working GP to make sure your solutions meet real world problems.

Our rigorous training includes GCP, GDPR , safeguarding, IATA training as standard and we will work with you to train the clinical team allocated to your trial with your bespoke additional training needs.

All allocated trial teams include trained staff who are ready to step in last minute, to allow for sickness or variations within your study.

Our research nurses are clinically proficient, and work alongside our team of nurses with specialist skills such as Tissue Viability.  We provide training to all our nurses to meet the needs of your trial

Home Care Clinical Trials

Our team work with each project from inception of the idea, support with trial design to ensure the best fit for your product and budget, work alongside you and clinical teams to develop protocols that are the right fit for you, but also pragmatic in their delivery.  For trials that crossover into community settings, our research nurses lead and manage the trial, liaise with clinical settings throughout the study, and provide continuity of care to participants, leading to good recruitment and retention of participants.

We only choose a limited number of trials per year, and work with you to make sure we are the right fit to be your trusted partner.  We have an ethos of honesty and transparency, and like to keep open channels of communication throughout the trial

Commercial confidentiality in trials and GDPR requirements around special category (health) data in the UK, makes the security of documents, patient information and communications forefront in our organisation.

We, unusually for most clinical companies, have a dedicated Data Protection Officer overseeing the information pathways, and a dedicated Senior IT manager, applying secure mobile device management technologies and data security technologies.  Our IT systems are accredited and audited by CyberEssentials Plus to meet the standards required to share NHS patient data.