ARO – University research organization

The Vall D'Hebron Research Institute created in 2014 the University Research Organization (ARO) platform with the aim of helping researchers and sponsors to develop clinical research in Vall of Hebron. The ARO platform offers a complete package on how to manage, from start to finish, the services that are needed to conduct clinical trials and studies. Thanks to its multidisciplinary team, this service can work as a complete contract research organization (CRO) service in clinical trials from phase I to IV within a wide range of possibilities. It also provides advice to the set of researchers and trial sponsors on how to achieve the best experimental design and organizational options to maximize resources. With the collaboration of other VHIR services, the ARO also participates in other aspects that help the development of research projects.

Institutional Contacts / Head of Facilities

MR

Marta Rosal FontanaPreclinical Core Facilities Coordinator
Vall d’Hebron Institut de Recerca (VHIR)

Provisional Contacts

Olga Sánchez-Maroto Carrizo | Head of Unit |  olga.sanchezmaroto@vhir.org  | 671 105 528 ext29747

Olga Sánchez-Maroto Carrizo |  olga.sanchezmaroto@vhir.org  | 671 105 528 ext29747

Albert Barberà Lluis (Director of Advanced Therapies Hub and Technological Platforms) |  albert.barbera@vhir.org 

CERCA Institutes

Owners

Centres CERCA List

Equipments & Services Offered

Start-up activities: Guidance, analysis and development of research projects. Analysis and development of documentation for the project. Obtaining the EudraCT number. Approval of the management of the part of the ethics committees and regulatory bodies. Support regarding contract management. Documentation management (general study archive and researcher archive). Public record of the clinical trialss Supplier management (insurance, printer, etc.). List of random distribution. Project execution activities: Project management and control of project progress. Control of activities (initiation, follow-up and telephone visits). Documentation management. Management of the approval of modifications by the ethics committees and regulatory bodies. Pharmacovigilance. Preparation and direction of the meetings and teleconferences of the researcher. Maintenance of the public record of the clinical trial. Drug management. Management of study materials. Management of study samples. Data management. Statistical analysis plan. Completion activities Data management. Data entry. Control of activities (completion visits). Statistical reports. Clinical report. Preparation and direction of researchers’ meetings and teleconferences. Maintenance of the public record of the clinical trial. Drug management. Management of study materials. Management of study samples.

Categorització

RIS3CAT domains & other

RIS3CAT Domains
CERCA GINYS Categories

GINYS-VHIR-009

Access procedure & Fares

Institutional Networks