Scientific Service Responsible Person

Legislative Decree no. 219 of 24 April 2006, implementing Directive 2001/83/EC, provides for that each Marketing Authorisation (MA) Holder of medicines is bound to have in place a scientific service entrusted with the delivery of information on the marketed medicines.

Such service should be supervised by a graduated Responsible Person (Scientific Service Responsible Person) adequately trained, as described in the Decree.

Di Renzo Regulatory Affairs has a special unit dedicated to the promotion of medicinal products for human use and to Scientific Information, including more experts qualified to take on the role of Scientific Service Responsible Person on behalf of third companies.