Execution Of Your Clinical Studies At Our Sites
Our network of Sites and PIs with their robust patient databases is ready to help you execute your Clinical Studies in an efficient and reliable manner.
Clinical Sites Network
Cooperate with network of experienced investigators and sites focusing on Neurology, Endocrinology and Obesity in the Slovak Republic.
Our Clinical Services
We are here to improve patients' lives by simplifying the daily operations of pharmaceutical companies and CROs conducting clinical studies.
Formation Of New Sites
We have processes in place to find you a new approved site in your chosen therapeutic area with a qualified and trained PI within weeks.
Whatever You May Need
Do you need a different kind of help with conducting your studies in Slovakia? Just let us know, we might be able to help you.
Multiple Sites and Investigators under One Roof
Central Europe Research is a dedicated network of clinical research sites and investigators across western Slovakia, devoted to providing reliable, high-quality, and efficient clinical trial services. Specialising in neurology, endocrinology and obesity therapeutic areas, our focus ensures predictable patient recruitment, robust data integrity, and compliance with international regulations.
With experienced investigators, extensive patient databases, and in-house legal support, we offer pharmaceutical companies and CROs a dependable and streamlined research environment and guarantee swift contract processing. Our expertise, coupled with comprehensive regulatory knowledge and patient-centric methods, ensures successful and smooth trial execution.
Why Choose Central Europe Research?
Discover compelling reasons to partner with us for your clinical trials.
Focused
Expertise
Deep specialisation in neurology, endocrinology and obesity ensures effortless adherence to protocols and investigator brochures.
Patient Recruitment
Efficient and reliable patient recruitment for successful study outcomes. Robust interconnected patient databases allows for efficient enrolment.
Regulatory Compliance
Strict processes and robust documentation, both managed centrally, help all parties to stay compliant with applicable regulations and clinical standards.
Joint Management
Management of the trial on a site level. Joint management of the activities performed by all involved sites and investigators from our network. Fast turnaround time on the paperwork.
Who will be taking care of your clinical trials?
Mgr. Enriko Maliňák
Founder
Enriko, who founded Central Europe Research, is an experienced lawyer with several years of expertise in multi-center clinical trials involving both drugs and medical devices across Europe, gained through his work with a Nasdaq-traded biotech company and an EU-based medical device manufacturer.
MUDr. Eva Némethová, PhD
Site Leader and Investigator
Eva Némethová, M.D. is an experienced doctor in the field of endocrinology and obesity with years of clinical expertise and decades of private practice. She owns and operates her own clinical site with a robust patient pool and keeps the regular contact with the patients.
MUDr. Roman Mego
Investigator
Roman Mego, M.D. is a doctor with more than 30 years of experience in the field of pediatric neurology. He works in a private neurological center for children and adults. Professionally, he focuses on the issues of epilepsy, cerebral palsy, migraine and neuromuscular diseases, electroencephalography and eletromyography.
MUDr. Monika Horváthová
Investigator
Monika Horvath. H., MD, is a physician with over 30 years of experience in neurology. For over 20 years she has been treating adult and pediatric patients in the outpatient clinic, focusing on epilepsy, migraines, and various chronic disorders of the central and peripheral nervous systems.
Frequently Asked Questions
Your common concerns addressed with clarity and assurance.
What areas of research do you specialise in?
Currently we specialise in Neurology, Endocrinology and Obesity. However, we will be adding other therapeutics areas shortly.
If you are having troubles finding sites or PIs in a specific therapeutical area, let us know and we may be able to help you establish a new one.
How do you ensure patient recruitment?
We leverage extensive interconnected patient databases and established networks, ensuring reliable and predictable patient recruitment for our clinical studies. We are able to utilise patient databases across our network, which multiplies our chances for successful patient enrolment.
How quickly can contracts be processed?
With an in-house counsel on our team we can guarantee a turnaround time of 48 hours on most of the legal documents.
What regulatory standards do you adhere to?
We strictly comply with international regulatory and clinical standards as well as with applicable international and local legislation ensuring rigorous data integrity and compliance throughout the trial process.