Reaping the benefits of eCONSENT for clinical trials
Reaping the benefits of eCONSENT for clinical trials Clinical research is made possible because patient volunteers give their consent to participate in clinical trials. Informed consent is an essential part of enrolling patients in a clinical trial.  Through the consent process a potential participant receives all the information they need about their role in the clinical trial.   eCONSENT While in the past consent was acquired
Cromos Pharma on the upcoming implementation of EU Clinical Trial Regulation
Cromos Pharma on the upcoming implementation of EU Clinical Trial Regulation The long-awaited European Union (EU) Clinical Trial Regulation (Regulation (EU) No 536/2014) (CTR) will come into effect in early 2022. The CTR is intended to improve the submission and review processes for clinical trials via a centralized portal. In recent weeks, the European Medicines Agency (EMA) has confirmed that the clinical trial EU Portal and Database, the
World Hepatitis Day and the role of clinical research
World Hepatitis Day and the role of clinical research Hepatitis is an inflammation of the liver, most commonly caused by viral infection. One of the world’s leading causes of death, viral hepatitis kills as many people worldwide as HIV/AIDS, malaria or tuberculosis. In 2019, WHO estimated that hepatitis B and C caused the deaths of 1.3 million people. Ahead of World Hepatitis Day on July 28,

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