Services

A range of services that guide and support the costumer during the whole process.
OUR EXPERTISE AT YOUR SERVICE

How can we
HELP?

Ask to our Team for a meeting, they will know how to meet your needs!


Clinical Trial

Rely on us for the management of your clinical trial!


Strategic Consulting

Our strategies and our methodological approach, allow you to receive a focused and a specific consult based on your need


Training Courses

We organize training with qualified and expert teachers


DATA ANALYTICS

Strategic Consulting in Clinical Projects


Creation, coordination and management of Scientific Boards: creation and implementation of surveys, training courses, editorial paths, opinion papers, guidelines. All our Know How is at your disposal to help you to reach your goal.



REAL DATA

From clinical trials to clinical practice


The observation of what happens  opens new opportunities for patients.



EXPERTISE YOU CAN COUNT ON

Publications


Our strong background in clinical research and our rigorous methodology will allow you to publish on high impact factor journals.



360° Clinical Research



Study Setup
Startup
Project Management
IMP Production, storage, distribution and return*
IMP Management
Central Lab selection and management
Monitoring (onsite and remote)
Auditing
Certified and proprietary eCRF
Data Management
PharmacoVigilance*
Biometrics & Statistics
Medical Writing
Publishing



FullCro & Alliance on Excellence Consortium (ACE)


This group of handpicked CROs (Fullcro included) allows to take advantage of geographical or indication-related specialization, without the disadvantages of big full-service CROs, the ACE consortium provides:

  • Proven and estabilished investigator network in several indications
  • Advantage as speed of start-up timeline and solid feasibility of recruitment strategy ensured by recent performance metrics
  • Innovative, efficient and fit-for-purpose Operational Strategy aiming at involving the countries with the shortest start-up timeframe and guaranteed recruitment strategy


Real World Evidence

Survey / Real life

A “Quick and Smart“ tool abel to rationalize medical data concerning pathologies managment in clinical practice


CLINICAL TRIAL / REGISTER

Support for the authorization process
Appropriate eCRF and “user-friendly“
Exisisting database analysis for feasibility (raw data or aggregated) and collection




SURVEY / DELPHI

Scientific board coordination
Survey/Delphy realization
Statistic report presentation




Scientific Advisory Board



Strategic consulting

  • Risk/Benefit evaluation: identify root causeand rank interventions
  • “Life vest”for critical phases in clinical project
  • Methodological support to transform a scientific insight in a successful clinical/scientific project
  • Biostatistical feasibility and support in scientific project design
  • ICT digital solution customized on projects
  • Foundraising opportunity



Dedicated Team

Medical writing & Publishing

Dedicated structure and coordinated by the Scientific Director, with 40 years of experience in scientific publishing and reviewer for Elsevier.
The unit counts on 4 Medical Writers and 2 biostatistics with extensive editorial experience

OUR AIM IS TO PUBLISH WHAT WE DO!



Training

Tailored Training for pharma company, CRO, and indipendent clinical units
Webinar session
Educational continuous training for professional key figures in clinical study



Contact fullCRO

We’re ready to offer the right sulutions for you and your team.


CALL US

+39.06.58.30.03.26
+39.06.58.30.03.27


FAX

+39.06.58.30.03.09


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we are your FULLCRO




+39.06.58.30.03.26
+39.06.58.30.03.27


Fax e mail

Fax +39.06.58.30.03.09
info@fullcro.org




Copyright by FullCRO 2019. All rights reserved.


Fullcro SRL - 12073321007 - copyright 2019