GCP training, for the people the evidence depends on.
ICH E6(R3) training tailored to who's actually doing the work, clinical sites, investigators, study coordinators, sponsor study teams, and the nutrition and consumer-health teams that historically operate outside classic pharma GCP.
The work, made concrete.
Not a service brochure, the actual scope, the actual deliverables, and how it plugs into ECS®.
- Clinical sites & investigator teamsSite readiness, delegation log, source data, informed consent workflow, SAE reporting, everything an investigator team needs to pass an inspection.
- Sponsor study staffSponsor obligations under ICH E6(R3): oversight, quality management, vendor oversight, TMF completeness, safety reporting.
- Nutrition & CHC teamsGCP applied to non-Rx contexts, FSMP, botanicals, functional food, OTC, where the requirement exists but the training rarely does.
- Investigator-Sponsored Study PIsThe GCP baseline for PI-run studies, so an academic protocol survives ethics and authority review.
Every deliverable has a name on it.
What you receive.
Every engagement lands with named artefacts you can use.
- On-site workshop, live remote or async modules, matched to the audience
- Individual training certificates and a maintained training log
- Site-readiness memo highlighting gaps and remediation actions
- Follow-up Q&A window after the training
Teams trained on GCP by Evidilya land in ECS® already speaking the same language, source data, monitoring plan, TMF and audit trail all map to what they've been trained on.
Three moments this service earns its place.
If any of these describe where you are, this is the right entry point.
- Moment 01
An ethics committee has asked for GCP conduct and the site team is ready for formal training.
- Moment 02
You're a sponsor running a first nutrition or consumer-health trial and need your study staff GCP-ready.
- Moment 03
You're preparing a PI-sponsored study and want it inspectable from day one.
Often engaged together.
Evidence strategy & study design
Map the evidence path, position the product scientifically, and design protocols and endpoints across every domain and product class.
Learn moreMonitoring & RBQM
Quality by design across the whole study, not monitoring alone: risk assessment, on-site, remote and centralised oversight against your risk plan, corrective actions tracked on ViSA.
Learn moreInvestigator-Sponsored Study (ISS) support
You have the idea. We give you the CRO engine, à la carte, to design, run and publish.
Learn moreTalk to the team about this service.
Tell us the study or the question, we'll come back with a scoped answer.