Conference in Madrid: “CTIS: full application of the European regulation of clinical trials”
The experts participating in our conference agreed to value the CTIS as a tool that will be very useful for the management of clinical trials in Europe, by harmonizing the requirements among different countries and centralizing documentation management
Sermes CRO, first company to manage the submission of a clinical trial in Spain through CTIS
Sermes CRO, together with Mikrobiomik, manages the first submission of a clinical trial in Spain through CTIS (Clinical Trial Information System), the new European clinical trial’s portal.
Coping with missing values in clinical trials
When it comes to clinical trial statistical analysis, missing values are a major challenge that we need to address. Have they ever been a problem for you? If so, or if you just want to learn more about them, keep on reading!
Proud of Sermes CRO’s women workers
Women biotechnologists, doctors, pharmacists, biologists, chemists, psychologists, biochemists, engineers, veterinarians, and nutritionists… All of them are part of our staff and make us feel proud, every day, with their contribution of knowledge, their experience and their ability to produce new ideas for the improvement of clinical research processes
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!