The Sample Network's ability to rapidly collect biosamples is built on our established global network of rigorously vetted clinical sites, and dedicated study teams.
Each site has been assessed for rapid study initiation, access to participants, adherence to protocols, ability to use standard or client specific collection kits and timely study completion.
Our pre-existing ethical approvals for scientific and health related research allows exceptionally fast initiation of studies, often within a week of purchase order and subsequent high collection rates that can mean some studies can complete within a few weeks.
Taken together, this has allowed many of our collaborators to accelerate research and development timelines, and subsequently move forwards their technologies and products for patient benefit.
We begin by deeply engaging with your scientific team to fully understand your biosample needs.
This could include clinical parameters, sample processing requirements and data requirements
We support all complexity levels of request from those who have detailed protocol requirements to those with sample only requirements.
Based on the requirements denoted we select our sites that we have previously determined are able to collect in those indications, and calculate collection rates and costing.
Once complete we provide documents outlining the sample requirements in detail (biosample, disease inclusion and exclusion, processing and data requirements), alongside the estimated time to completion and cost per sample.
Once contracting has completed, we commence collection, often within one week of agreement finalisation. We provide all kits and materials, unless requested by the client (such as custom kits).
During the collection we provide regular updates on progress, and notify on whether any additional points come up during collection.
On completion, we take care of logistics of the samples to your organisation (anywhere in the world), and provide the associated data manifests digitally.