The smart and ethical choice for your project

We offer customized consulting, targeted training, simple and effective solutions
for developing and managing clinical trials with drugs and medical devices.
We collaborate with clinicians, scientific societies and
public and private companies in health care,
national and international CROs.

We use effective strategies, fluid communication and performance indicators to supervise the correct progress of the project and to identify and mitigate risks in advance. Our goal is to complete each project on time and on budget, ensuring a high quality.
We manage submissions and contract negotiations by complying with the documentation and time requirements of authorization practices. We develop strategies to identify issues in advance, collaborating with relevant authorities.
We support you in writing the protocol, the key document of the clinical trial. We draw up, adapt or translate into local language other study essential documents such as consents, operating manuals, clinical study report. We carry out bibliographic research, we write abstracts and manuscripts.
The role of the site is essential for the success of the project, especially in non-profit studies. We offer you organizational tools, study-specific toolkits and targeted training to manage all phases of the clinical trial in a simple and effective way.
We operate with high quality standards. We follow every step of the clinical trial to ensure the presence and the respect of adequate procedures and records to obtain high quality data. We provide support in the implementation of a quality system tailored to different needs and compliant to required standard.
We offer assistance in the proper and accurate identification, management and retention of study records, as required by applicable law. We perform quality control checks on TMF both in progress and at the conclusion of the study.
We offer training targeted to different needs and professionalism. We provide both general courses on topics related to the world of clinical research and study-specific courses. We manage the organization of training events.

VIS Ethic Research was born from the passion
and decades of experience in clinical research of three women:
Vanessa, Irina and Silvia.
The strength of this new company is given by the multidisciplinary skills
of the members and by a shared ethical approach
to the world of clinical research.

Vanessa Bacchi - Start-up Unit & Administrative Manager

In 2007 she joined the world of clinical research. Since 2009 she has been responsible of Trial Start Up Unit of a CRO for the authorization requirements of interventional and observational studies with drugs and clinical investigations with medical devices. She also dealt with the management of drug supply to sites, she was a trainer in theoretical courses on clinical trials and responsible of organizing events.

Irina Mantovani - Scientific Director & Project Manager

Graduated in Biological Sciences and Specialized in Clinical Pathology, she entered the field of clinical research in 2006 and until 2014 she was Trial Coordinator of clinical trials in hematology and oncology. Later she plays the role of Project Manager in a medical device company for orthopedics and then in various Italian and international CROs, dealing with clinical trials with drugs in various therapeutic areas.

Silvia Cellini - Project & Quality Assurance Manager

Graduated in Chemistry and Pharmaceutical Technologies, with a PhD in Pharmacology and Experimental Oncology, took part in the II level Master of the School of Clinical and Epidemiological Research and in the Executive Master in Project Management. Lecturer in the Master in Clinical and Epidemiological Research and Quality specialist at a leading Italian company in laundering & sterilization services. Since 2007 she has worked in different CROs covering various roles: CRA, national and international Clinical Project Manager and Quality Assurance Manager.