Wherever you are in the world, we are here as your eyes and ears and to keep you connected.
We can provide a full suite of clinical trial services from site feasibility, site and vendor selection through to your final CSR (and all the fun stuff in between).
With our extensive local expertise and established network relationships, we provide site feasibility, assessment and strategic advice.
We offer complete clinical project management of study trials both locally and as part of a global solution.
On the ground clinical team provides on-site visits
-Qualification, Initiation and ongoing Monitoring-
& supports remote monitoring requirements.
INVESTIGATIONAL SITE SUPPORT & MONITORING
Our wider clinical team provide critical review and input into eCRF databases from a real-world and experienced perspective.
DATABASE REVIEW & SUPPORT
Our expert team manages ethics submissions and development of supporting packages, preparation of clinical trial plans and study documents.
CLINICAL TRIAL DOCUMENTATION
We provide a flexible approach to TMF management, whether it is an internally managed and maintained TMF (including e-solutions) or a client preferred third party.
All projects are underpinned by quality reviews throughout the life-cycle of a trial, with regular reviews of trial data and outputs, risk assessment, analysis and management, and regular sop development, training and adherence.
We tailor our services to your needs, whether you need to outsource all components of clinical delivery, or whether only certain functions are required. Our flexible and adaptable approach is a core value of Beyond, where we are here to meet your needs and expectations.