SermesCRO is a full CRO (Contract Research Organization), providing quality clinical research services for 26 years. We partner you through the hole drug development cycle: from early phases, to post-marketing studies. Based on a strong scientific, therapeutical and regulatory expertise, we will keep your study on track. It will be delivered within time, quality and profitability targets.
 
We provide a comprehensive range of services to fulfill any global CT needs: clinical operations, start up, pharmacovigilance, legal representation, regulatory advice, data management and qualified outsourced staff.
 
We are an experienced partner in EMA’s new Clinial Trial Information System (CTIS), as part of it’s working group since 2017.
 
Our Advanced Therapies Unit provides counseling on regulations and regulatory requirements from the outset and throughout the research Project.
 
Our Artificial Intelligence and Big Data Unit provides unique clinical research data, expert analysis and innovative business intelligent solutions.

Clinical Trials

Health Data

Life Sciences

Sermes CRO

Antonio Berlanga Ruiz

Marta Manso Zamorano

Jose Alberto Catala Hernansaiz

The Technical Roles team at Sermes CRO is pivotal in managing technical aspects of clinical research projects. This team includes experts in Trial Master File (TMF) management, data science, site reliability engineering, drug safety, and quality assurance. They ensure that clinical trials run smoothly by handling data analysis, maintaining data integrity, overseeing drug safety procedures, and ensuring compliance with regulatory standards.

Technical Roles

About

Team members

Other teams at Sermes CRO

Administrative Team