Clinical Trials Adverse Event Processing

Clinical trials play a crucial part in any drug development life cycle where it is key to gain information on a product’s safety profile. The PharmaLex international team of clinical safety experts, with large expierence in the management of clinical safety activities, effectively supports sponsors with Pharmacovigilance activities during clinical trial development programmes. PharmaLex designs and implements clinical trial safety procedures allowing sponsors to properly identify, manage and monitor the safety information of products involved in clinical trials. Also, PharmaLex ensures compliance with global and local regulatory requirements regarding clinical safety data processing and submissions.