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.
read moreFlexible 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
23% Ph I-II 52% Ph III 25% Ph IV - VI
260 GXP Audits 50 Mock Inspections 40 Due Diligence
Clinical Trials, Auditing and Consulting Projects
Auditing and Consulting Projects
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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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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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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