Non comercial clinical trials

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

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

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

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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

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