Clinical Trials Solutions
Clinical trials solutions, tailored to your needs.
Clinertia supports the people and organisations behind clinical trials. We provide practical consultancy and project-based services to sponsors, Contract Research Organizations (CROs), Site Management Organizations (SMOs), investigators, hospitals and research sites.
Our services
Whether you are developing a new study, preparing a site, strengthening documentation or looking for specialist support, we help you identify and coordinate the work needed to move forward.
- 01
Study planning & feasibility support
Operational planning, feasibility documentation, workflow mapping and study-start-up coordination.
- 02
Protocol & scientific document development
Protocol writing support, study synopses, informed consent forms, study manuals, standard operating procedures and other trial documents.
- 03
Regulatory & ethics submission readiness
Preparation and review of submission documents, completeness checks, document tracking and query-response support. Formal submission or regulatory representation is performed by the appropriately authorised party where required.
- 04
Site set-up & readiness
Site needs assessments, essential-document organisation, equipment and vendor coordination, and research-team training.
- 05
Trial procurement & logistics coordination
Sourcing support for approved trial supplies, equipment, background/concomitant medicines and service providers, subject to applicable procurement, import and product requirements.
- 06
Patient recruitment support
Recruitment strategy, participant information materials and outreach planning, subject to ethics approval, privacy requirements and sponsor/site oversight.
- 07
Quality management support
SOP development, documentation review, process mapping, quality gap assessments, CAPA documentation support and audit readiness.
- 08
Training & capacity building
Tailored clinical research, research coordination, documentation, ethics and GCP-related training. Any formal certification is offered only when appropriately authorised.
- 09
Research network & vendor coordination
Connecting relevant sponsors, CROs, SMOs, investigators, research sites, laboratories and specialist vendors.
Next step
Discuss your trial requirements.
Tell us what you are working on — a new study, a site to prepare, documentation to strengthen. We’ll discuss your requirements and the most suitable next step.
Services are scoped to your project needs, responsibilities and applicable regulatory requirements.