About Us

We are leading full-service CRO specializing in clinical research in CEE and global clinical consulting. Clinmark is commited to providing support for pharmaceutical and biotechnological companies in the area of research and development through operational activities, professional auditing, consulting and education.

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Testimonials

Flexible and cooperative, willing to provide service according to client's expectations

Regional Head of Operations
American Pharmaceutical Company

Flexible and cooperative, willing to provide service according to client's expectations

Regional Head of Operations
American Pharmaceutical Company

Flexible and cooperative, willing to provide service according to client's expectations

Regional Head of Operations
American Pharmaceutical Company

Tell us where you are - we will assist you

product development plan
preclinical development
early clinical development phase I, II
late clinical development phase III
marketing authorisation
post-authorization development

230+ Clinical Trials in Europe

23% Ph I-II 52% Ph III 25% Ph IV - VI

19 600+ Enrolled Patients

Medicinal Products Medical Devices Nutritions Supplements Cosmetics

350+ Consulting Projects Worldwide & 230+ Clinical Trials in Europe

260 GXP Audits 50 Mock Inspections 40 Due Diligence

Clinical Trials, Auditing and Consulting Projects

Auditing and Consulting Projects

Ready to Assist You!

News

CLINMARK celebrates International Clinical Trials Day
20 maja, 2022

20th of May is celebrated as International Clinical Trials Day. The date of May 20 was chosen to commemorate the day James Lind began his study to determine the causes of scurvy - a study considered the first randomized clinical...

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CLINMARK at OCT Barcelona 2022
17 maja, 2022

We would like to thank you for very interesting time and welcome you during two exciting days of meetings at Outsourcing in Clinical Trials conference in Barcelona.  After a break of 3 years, it was a great pleasure to meet...

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Clinical trials – Why are they so expensive?
25 marca, 2022

It’s a pretty common knowledge that clinical phase of drugs or medical device development is an expensive project. From drug development to medicinal product dossier submission to EMA or FDA, through investigative sites’ costs or implementation of IT solutions, the...

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