Non comercial clinical trials

Clinical Consulting helps in the organization and conduct of non-comercial Clinical research (academic trials).

The role of the CRO is to conduct research in terms of:

Data quality assurance

Monitoring the study

Verifying the correctness of the data against the source documentation

Help investigatos and research teams

Support for clinical trial documentation including:

Study protocol

Investigator's Brochures

The Informed Consent Form (ICF)

and Information form for the patient

Get more details

Administrative support:

perform comprehensive site management and monitoring activities to include the following types of monitoring visits:

Complete the necessary documents

Application submission to EC and CA

Keeping correspondence with EC (KB) and CA (URPL)

Trainings

Good Clinical Practice (GCP)

Study specific trainings - procedures

Principles of keeping source documentation

Data entry to the database (CRF)

Cooperating Universities

HEADQUARTER

ul. Dzwonkowa 104

43-100 Tychy, Poland

+48 32 227 20 05

office@clinicalconsulting.pl

WARSAW OFFICE

Al. Jana Pawla II

27 00-867 Warszawa, Poland

+48 32 227 20 05

rental@clinicalconsulting.pl

Clinical Consulting is now Aurevia

Clinical Consulting is joining forces with Labquality, Artimed, Kasve and Prisma CRO as Aurevia, a newly merged company of experienced experts advancing healthcare and pharmaceutical and medical technology development.

Aurevia is a full-service contract research organization (CRO) and a regulatory affairs and quality assurance expert experienced in pharmaceuticals, Medical Devices, in vitro diagnostic devices and combination products, but also a trusted EQA partner and auditing provider.

Learn more about Aurevia: aurevia.com