BIOSIMILARS: REGULATORY ASPECTS IN THE USA AND THE EU
- At: AbuDhabi (United Arab Emirates) (2019)
- Type: Poster
- Poster code: POS-RSC-005
- By: KHALID, Garba Mohammed (Università degli Studi di Milano, Department of Pharmaceutical Sciences, Italy)
- Co-author(s): Garba Mohammed Khalid: Department of Pharmaceutical Sciences, Università degli Studi di Milano, Milan, Italy
Paolo Rocco: Department of Pharmaceutical Sciences, Università degli Studi di Milano, Milan, Italy
Paola Minghetti: Department of Pharmaceutical Sciences, Università degli Studi di Milano, Milan, Italy - Abstract:
Background
The high cost of biotechnological medicinal products and the increasing number of patent and data protection expirations is motivating manufacturers to develop biosimilar products and physicians to prescribe them, either spontaneously or due to payers’ policies (non-medical switch or constrained prescription). Unlike generics, biosimilars
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Last update 28 September 2023