We have a data base of Investigators by specialty, which have been certified in Good Clinical Practices and have experience handling clinical studies. This previous experience provides them the knowledge that is only acquired through practice.
Our Study Coordinators pool has personnel with the corresponding accreditations, as well as the necessary experience supporting different types of research projects and executing in compliance with Good Clinical Practice.
Study Drug Logistics
We are facilitators in the process of import, distribution to investigational sites and destruction of study drug, under the standards required by local legislation.
Study Drug Storage
We guarantee the storage and inventory control of study drug in depots that comply with quality, physical conditions (temperature and humidity), security, reliability and accountability requirements.
We have a Clinical Diagnosis and Research Laboratory with renowned experience complying with Good Laboratory Practices, under ICH guidelines. The Laboratory´s ultimate objective is to execute their work with excellence, precision and in time.
We facilitate the hiring of Clinical Monitors qualified to oversee data collection and investigational site execution, ensuring regulatory compliance. Our Clinical Monitors have previous audit experience.
Qualified personnel that manage the regulatory process (submission and follow-up until final approval) and the files for regulatory documents (Trial Master File).
Running a feasibility evaluation properly designed, allows the correct strategy in selecting the most suitable sites for the execution of a research project.