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...
On July 31, 2021, the European Commission announced the full functionality of the EU portal and database, the Clinical Trials Information System (CTIS) in the Official Journal of the European...
One of the objectives of the Regulation No 536/2014 is to increase the transparency of clinical trials among the general public. The public access to the data of...
More than 130 years after discovering and naming of the Plasmodium parasites behind malaria, the world now has its first approved vaccine against them. Many malaria researchers have...
The process of obtaining authorization to conduct a clinical trial involves appointment of a Reporting Member State (RMS). In multinational clinical trials, at the same time as submitting the application dossier...
The discussion about future vision of clinical trials started, from the very first day when Decentralized Clinical Trials (DCT) were mentioned as a method worth consideration for the...
We are only days away from the entry into force of the Regulation No 536/2014 on clinical trials on medicinal products for human use, which repeals clinical trials Directive 2001/20/EC. A lot...
This holiday season, we at Clinmark pause and take advantage to express our gratitude and appreciation to all our Friends, Clients and Partners for cooperation with us.Working with...
We are thrilled and pleased to announce that Clinmark has been nominated as one of 10 Most Reliable CRO’s to Watch in 2021 by Insightscare! For us being...
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