Since 2004, when Distefar was created, it has established itself as a reference partner in the Comprehensive Management of Clinical Trials.
Our team is composed of pharmacists and professionals who are duly qualified and in continuous training.
In its origins, Distefar was responsible for the management of drugs in the field of national and European research, meeting the needs of Laboratories, CROs, Foundations and Hospitals.
Over time we have been increasing the portfolio of services, adapting to the needs of our customers, thus consolidating our position within the investigation. Always providing innovative solutions, thus facilitating the work to our customers and establishing strong and lasting ties.
Our goal is and will remain, to achieve excellence, to carry out your project successfully
“Our code of conduct on data protection in clinical trials and pharmacovigilance is a benchmark for the future European code”.Farmaindustria’s self-regulation document is the focus of a scientific meeting organised by the Royal National Academy of Pharmacy. Source: www.farmaindustria.es Less than a month ago […]