Bringing the study to the participant is why our evidence arrives faster, and why it arrives with a lighter footprint. Our sustainability programme runs on the four pillars an EcoVadis assessment looks at, and Evidilya is EcoVadis rated.
EcoVadis assesses environment, labour and human rights, ethics and sustainable procurement. We treat the assessment as an external check on progress rather than a badge, alongside the ISO 9001 certification that governs how our studies run.
The lowest-impact study visit is the one that never needed a journey. Direct-to-Participant execution removes avoidable participant travel; electronic source, eConsent and remote monitoring remove paper and monitoring flights; sample logistics and cold chain are planned for the shortest viable route.
Fair employment, safe working conditions and no tolerance for forced or child labour, inside Evidilya and along the supply chain. Particular attention goes to field personnel, home-visit nurses and couriers who work outside our offices.
Anti-corruption, scientific integrity, conflict-of-interest management, data protection and a protected speak-up channel. These are not a parallel programme: they are the Code of Ethics, applied.
Suppliers, sites, laboratories and technology partners are assessed on environmental and social performance alongside quality and price, with the expectation of improvement over time.
In a conventional trial, most of the environmental and human cost sits in movement: participants travelling to sites, monitors travelling to sites, paper travelling everywhere. That is exactly the cost our operating model was built to remove.
Home visits, telehealth and community pharmacy touchpoints replace repeat trips to a distant specialist centre, for the participant and often for their carer too.
eConsent, electronic source and e-signatures remove printing, courier runs and archive boxes across the study lifecycle.
Centralised monitoring against a documented risk plan replaces routine on-site visits, cutting travel without cutting scrutiny.
Sample routing and kit distribution are planned around the participant's location, reducing distance, dry ice and wastage.
Reaching people who live far from research is a social outcome, not only an operational one. Designs keep a non-digital pathway open so participation is not a privilege.
Minimisation and defined retention mean we hold what the science requires, for as long as the protocol and the law require, and no longer.
We publish the mechanisms, not modelled savings. Where a sponsor needs a quantified footprint for a specific programme, we build it from that study's own logistics data.
Social performance is not a poster in a corridor. It is whether a nurse on a home visit can stop an unsafe activity, whether a junior scientist can flag a data-integrity problem, and whether either of them still has a career afterwards.
Retaliation against anyone who reports in good faith is treated as a breach in its own right, investigated by people without a conflict in the matter, and closed with a documented outcome.
Participant protection, scientific integrity, anti-bribery, data protection, responsible AI and enforcement. Thirteen pages, readable on-site.
Read the Code →The ISO 9001 certified quality system, ICH E6(R3), ALCOA++ data integrity and inspection readiness.
How quality runs →Confidential and anonymous reporting, in line with EU Directive 2019/1937 and its national implementations.
Open the channel →Send the questionnaire. Sustainability, quality and data-protection due diligence are handled by the same Expert team that would run your study.
