Studying at the University of Verona

Here you can find information on the organisational aspects of the Programme, lecture timetables, learning activities and useful contact details for your time at the University, from enrolment to graduation.

Study Plan

This information is intended exclusively for students already enrolled in this course.
If you are a new student interested in enrolling, you can find information about the course of study on the course page:

Laurea magistrale in Molecular and Medical Biotechnology - Enrollment from 2025/2026

The Study Plan includes all modules, teaching and learning activities that each student will need to undertake during their time at the University.
Please select your Study Plan based on your enrollment year.

1° Year

ModulesCreditsTAFSSD
One course to be chosen among the following
One course to be chosen among the following

2° Year  activated in the A.Y. 2021/2022

ModulesCreditsTAFSSD
Training
2
F
-
Final exam
40
E
-
activated in the A.Y. 2021/2022
ModulesCreditsTAFSSD
Training
2
F
-
Final exam
40
E
-
Modules Credits TAF SSD
Between the years: 1°- 2°
Two courses to be chosen among the following ("Biotechnology in Neuroscience" and "Clinical proteomics" 1st and 2nd year; the other courses 2nd year only)

Legend | Type of training activity (TTA)

TAF (Type of Educational Activity) All courses and activities are classified into different types of educational activities, indicated by a letter.




S Placements in companies, public or private institutions and professional associations

Teaching code

4S003677

Coordinator

Linda Avesani

Credits

6

Language

English en

Scientific Disciplinary Sector (SSD)

BIO/15 - PHARMACEUTICAL BIOLOGY

Period

Primo semestre dal Oct 4, 2021 al Jan 28, 2022.

Learning outcomes

The course aims to give the students notions of the use of recombinant systems for the production of biopharmaceuticals. In particular, the course will be focused on the biomolecular techniques used for the expression of recombinant proteins in prokaryotic and eukaryotic systems and the downstream processing and purification for their large-scale production. The different platforms used for the recombinant expression will be studied and compared. The different US and EU normative procedures for biopharmaceutical commercialization will be evaluated and compared. Specific examples of biopharmaceutical produced in recombinant systems and their therapeutic applications like for vaccines and antibodies will be discussed and studied.

Program

General introduction to the concept of Molecular farming
Definition of a biopharmaceuticals and drugs

• Route for biopharmaceuticals approval. The Clinical Trials
and the Regulatory Agencies. GMP definition Biosimilars and Bioequivalence
• Platforms for the heterologous production of recombinant proteins with a focus on the relative upstream processes

The main categories of biopharmaceuticals: Antibodies, Vaccines, Toxins and Hormones

• Heterologousexpressionofantibodies Toxin-based therapy

Active immunization: the vaccines
The clinical use of antibodies from pathogen defence to chronic diseases
Productionofvaccines Immunogenicity
Post-translational modifications Immunologicaltoleranceandoraltolerance
T-cells Biotechnology
The downstream processing
Production of peptides and their clinical and daignostic applications


• •
• •
• •
Techno-economic analysis for the production of recombinant proteins
Patent, Clinical Trials and Description of a Biopharmaceutical. TEA analysis development

Examination Methods

oral exam and written test

Students with disabilities or specific learning disorders (SLD), who intend to request the adaptation of the exam, must follow the instructions given HERE