How to manage transitional clinical trials to the new European online portal, CTIS
The European clinical trial regulation establishes a three-year transition period in order to adapt to the new clinical studies’ online portal. In this article you will learn how to manage the transitions of your studies. It is essential that the sponsors and the CROs actively collaborate with each other in the transition strategy regarding CTIS, according to the different phases over the next three years
Welcome to our new website
We are delighted to announce the launch of our newly redesigned website. It reflects who Sermes CRO is and what we are capable of. The new website is modern and easy to navigate, it gives a clear message about who we are and a full services list. Don’t forget to check out our new blog. Pharmaceutical companies, biotechnologists and anyone interested in clinical research will find interesting articles there!
Azur Global Nutrition relies on Sermes CRO’s technological solutions
Azur Global Nutrition, leader in specialized solutions focused on immunonutrition, had many biological samples and clinical information coming from its research and development projects. They needed to organize and manage it in a systematic way. Sermes CRO then designed and created a personalized web portal that integrates application at user level and database. This solution allowed Azur Global Nutrition to work more efficiently, always measure their results and control the main process indicators
We support OAFI’s osteoarthritis patient-centric strategy. Have you signed for their upcoming congress yet?
OAFI’s 5th International Osteoarthritis Patients Congress will take place in Barcelona, on October 14th and 15th. You are still on time to sign up!
Lidya Domínguez Burgo, appointed Clinical Research Director in Sermes CRO
Sermes CRO strengthens its Clinical Research services, appointing Lidya Domínguez as the new Clinical Research Director. Her career path has always been linked to clinical research for 15 years
The importance of statistical analysis in clinical trials
If you are wondering why clinical trials need a statistical analysis… If you want to learn about the role of people involved in data analysis and protocol elaboration… Read on!
Mercedes Ovejero, co-author of a new scientific publication on bipolar disorder
Mercedes Ovejero is a specialist in clinical trials data analysis, PhD in Psychology and associate professor of applied Psychology Statistics at the Complutense University of Madrid. Her new publication analyzes social and emotional cognition in first degree relatives of bipolar disorder.
Ethics Committees and CROs, a necessary pairing in clinical research
An interview with ANCEI, the Spanish National Association of Research Ethics Committees: “CROs play a preponderant role in the compliance of good clinical research practice standards. They perform an important function in a clinical trial start-up and in the proper monitoring of the conditions in which they are conducted”, explains the management board.
University collaboration agreement between Sermes CRO and Francisco de Vitoria University
Sermes CRO and Francisco de Vitoria University have signed a collaboration agreement to incorporate internship students, as well as hiring recent graduates from this university.
EMA certifies Sermes CRO as a key entity in the CTIS Training plan
Sermes CRO has been elected by the EMA as “Train of trainers” for the new Clinical Trial portal, CTIS (Information System).