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

Video Games Day
13 września, 2022

This was not an ordinary Monday in our Clinmark Office. As during this particular day we calebrated International Video Games Day. We had 2 game consoles and a lot of different games to choose from. In the main competition we...

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Medical Device Q&A MDCG 2021-6 / Regulation (EU) 2017/745 (Part 2)
09 września, 2022

Which regulatory pathway should a Sponsor follow to conduct a clinical investigation in the pilot stage (i.e. first in human, early feasibility) in accordance with the Regulation (EU) 2017/745 (MDR)? The MDR describes different types of clinical investigations that follow...

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Questions & Answers – MDCG 2021-6 / Regulation (EU) 2017/745 (Part 1)
20 lipca, 2022

What are the general differences and improvements related to clinical investigations under the new Regulation (EU) 2017/745 (MDR) as compared to the Directives 93/42/EEC and 90/385/EEC? Regulation (EU) 2017/745 (MDR) will progressively replace both Directives (93/42/EEC and 90/385/EEC) and their...

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