As all professionals involved in the pharmaceutical sector appreciate, the regulations regarding medicines are in constant evolution.

This has gradually led to a definition of a new and highly specialized role of Regulatory Affairs Manager. The management team of pharmaceutical companies, or a section of this group, is often not able to keep abreast of the continuing developments concerning the obligations and regulations that need to be implemented. Mindful of these company dynamics and the need for the various managerial groups to be familiar with the fundamental concepts of the regulations, Di Renzo Regulatory Affairs has created specific courses conducted by our experts.

These courses, principally aimed at managers, can be organized for individuals or groups either at our offices in Rome or Milan, or at the company headquarters, and deal with themes of general interest as well as specific topics proposed by the companies themselves.

Such as:

• Fundamental regulations regarding the medicinal, medical device, food supplements and biocide sectors
• What is pharmacovigilance
• How can we best organize internal regulatory activity and what can be conceded to outsourcing
• What is scientific information and what obligations does it entail