Contract Research and Consulting Organisation
After almost 25 years, the law on medical devices has changed. The "old" EU Directives (Medical Device Directive (MDD) 93/42 / EEC and Active Implantable Medical Devices Directive...
MOVEMBER 2022
23 listopada, 2022
November has been recognized worldwide as a month of solidarity with men facing prostate cancer and testicular cancer. It is not without reason that it is this month...
On November 11, 2022 our Clinmark Team participated in Independance Run Warsaw 2022! Our runners did their best and all compleated this run in great shape and time....
­čÄâHalloween at CLINMARK­čÄâ
31 pa┼║dziernika, 2022
What a day! What a team! What a spirit! We have celebrated Halloween at our office and our amazing team had great ideas how to dress up. We...
What is considered burdensome or invasive? Where the investigation would involve submitting subjects to procedures additional to those performed under the normal conditions of use of the device...
We are very happy and proud to be recognized as TOP 10 MEDICAL DEVICE CRO in Europe 2022. Successful clinical trial execution is built on the pillars of...
Video Games Day
13 wrze┼Ťnia, 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...
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)...
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)...
Promotions Announcement!
15 lipca, 2022
Having over 20 years of presence on the market, continuous growth, our organization has implemented its own successful employee development program which allows Clinmark to expand its operational...