EU- Directive “Falsified Medicines”
Commission Delegated Regulation (EU) 2016/161 of 2 October 2015 supplementing Directive 2001/83/EC of the European Parliament and of the Council by laying down detailed rules for the safety features appearing on the packaging of medicinal products for human use
Questionnaire for Customers of E-Pharma Trento S.p.A.
In order to have a clear status of our Customer’s Requirements and to correctly define the URS (User Requirement Specification) of our future system we kindly ask you to answer the questions as below.