Clinical trials in Poland

Esploro Clinical Research Center is a dedicated research site owned by Centrum Bocian which has over 16 years of experience in gynecology, endocrinology, andrology and infertility treatment in Poland and Latvia. Our sites are located in the main cities of Poland: Warsaw, Poznań, Katowice, Szczecin and Białystok and Latvia: Riga.

Information for sponsor/CRO

Why we conduct clinical trials?

Our goal is to provide medical services at the highest level using innovative medical technologies by experienced and professional staff in a friendly and safe patient environment.

Physicians experience 
in clinical trials

16 years

Physicians experience in clinical trials
Patients 
in our database

⁓ 100 000

Patients in our database
Number 
of physicians

31

Number of physicians

Why we are unique in the clinical research area?

Quick 
feasibility process
Quick feasibility process
Smooth contract 
and budget negotiation
Smooth contract and budget negotiation
Highly qualified investigators, medical and non-medical staff
Highly qualified investigators, medical and non-medical staff
Effective recruitment 
strategy and retention
Effective recruitment strategy and retention
Efficient 
study set-up
Efficient study set-up
Highest quality at every stage of the clinical trial
Highest quality at every stage of the clinical trial

Experience in clinical trials

Esploro Clinical Research Center has experience in conducting clinical trials in the field of gynecology, endocrinology, andrology and infertility treatment (phase II and III).

INDICATIONS PHASE
ART/ embryo implantation II&III
Endometriosis IIa
Vasomotor Symptoms in Menopausal Women III
IVF/ET III
IVF/ICSI III
Vasomotor Symptoms in Menopausal Women III
Testicular Safety in Active Inflamatory Bowel Disease II

Conducting clinical trials allow us to develop and improve the quality of offered medical services, increase patient satisfaction and contribute to the development of medicine.

OUR TEAM

We partner only with best in class Investigators, which are supported by a knowledgeable team of study nurses, and study coordinators. All of them are qualified by education and experience in performing phase II - IV clinical trials in compliance with Good Clinical Practice and applicable regulatory requirements. Our experienced and involved team allow to ensure the highest possible standards of clinical trials execution.

We have 6 fully equipped facilities and certified medical equipment necessary to conduct clinical trials:

Room for Investigational Medicinal Products
Room for Investigational Medicinal Products
Refrigerators and freezers
Refrigerators and freezers
Weighing scale with height meter
Weighing scale with height meter
Thermometers
Thermometers
USG machine
USG machine
ECG machine
ECG machine
Centrifuge
Centrifuge
Defibrylatory
Defibrylatory
Blood 
pressure cuffs
Blood pressure cuffs
Medical 
Laboratory
Medical Laboratory
Histopathology Laboratory
Histopathology Laboratory
Genetic 
Laboratory
Genetic Laboratory

Credentials

Our sites are certified by the International Organization for Standardization in scope of Quality Management System (ISO 9001:2015). Esploro Clinical Research Center provide a full range of services, from testing and screening to highly specialized medical procedures. All our laboratories have been accredited by Krajowa Rada Diagnostów Labolatoryjnych (KRDL). We cooperate with recognized and certified external entities only.

Patient centric approach in clinical trials

Patient safety is always our top priority, as well as conducting clinical trials in compliance with the highest international medical and ethical standards. Thanks to an individual approach to each patient, care and support throughout the process, we can guarantee effective recrutation of research participants. We believe that providing patients with the highest possible standard of care will contribute to a higher retention rate, better research results, and enhancement of patients’ lives.

Esploro Clinical Research Center guarantees close cooperation with CROs/Sponsors and reliable conduct of clinical trials. Looking forward to working with you.