Production, Legislation and Marketing of Biotechnological Medicines

A.Y. 2025/2026
7
Max ECTS
56
Overall hours
SSD
CHIM/09
Language
Italian
Learning objectives
The course is intended to cover principles and general requirements for the development of biotechnological medicinal products, from biopharmaceutics to the manufacturing of the final dosage form. References are made to the quality assays, compendial and not, to characterize the finished medicinal products Regulatory aspects relevant to production and marketing are also addressed.
Expected learning outcomes
At the end of the course, students are expected to know the relation among the specific properties of an active substance, dosage form, administration site and the therapeutic requirements in order to formulate a medicinal product complying the requirements of quality, safety and efficacy. Starting from the main chemical-physical characteristics of the active substance, the student will be able to propose the most suitable route of administration, manufacturing methods for biotechnological and advanced therapy medicinal products to according to the Good Manufacturing Practices.
Single course

This course cannot be attended as a single course. Please check our list of single courses to find the ones available for enrolment.

Course syllabus and organization
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