Duration
Concepts and production of protein and oligonucleotide biopharmaceuticals : 15h Th
Living biopharmaceuticals and vaccines - part A: concepts and biosecurity : 6h Th
Living biopharmaceuticals and vaccines - part B: managing the risk of the release of cell and genetic products : 3h Th
Formulation of biopharmaceuticals : 15h Th
Quality control and analytical techniques in biopharmaceuticals, good practice, and legal recommendations - part A: analytical methods : 10h Th
Quality control and analytical techniques in biopharmaceuticals, good practice, and legal recommendations - part B: post-translational modifications : 3h Th
From the laboratory to the pharmacy: legal requirements - part A: patents and industrial protection : 5h Th
From the laboratory to the pharmacy: legal requirements - part B: specifics of regulation around biological drugs including advanced therapies : 5h Th
From the laboratory to the pharmacy: legal requirements - part C: procedure for releasing batches and the legal framework of vaccines : 1h Th
From the laboratory to the pharmacy: legal requirements - part D: introduction to biobanking : 3h Th
Number of credits
| Advanced Master in Industrial Pharmacy | 7 crédits |
Lecturer
Concepts and production of protein and oligonucleotide biopharmaceuticals : David Vermijlen
Living biopharmaceuticals and vaccines - part A: concepts and biosecurity : Véronique Fontaine
Living biopharmaceuticals and vaccines - part B: managing the risk of the release of cell and genetic products : Roland Marini Djang'Eing'A
Formulation of biopharmaceuticals : Rita Vanbever
Quality control and analytical techniques in biopharmaceuticals, good practice, and legal recommendations - part A: analytical methods : Marianne Fillet
Quality control and analytical techniques in biopharmaceuticals, good practice, and legal recommendations - part B: post-translational modifications : Cédric Delporte
From the laboratory to the pharmacy: legal requirements - part A: patents and industrial protection : Patrick Di Stefano
From the laboratory to the pharmacy: legal requirements - part B: specifics of regulation around biological drugs including advanced therapies : Hugues Malonne
From the laboratory to the pharmacy: legal requirements - part C: procedure for releasing batches and the legal framework of vaccines : Lorenzo Tesolin
From the laboratory to the pharmacy: legal requirements - part D: introduction to biobanking : Stéphanie Gofflot
Language(s) of instruction
French language
Organisation and examination
All year long, with partial in January
If a student fails an examination during the first term:
- They are permitted to resit the assessed subject during the second term (May-June);
Schedule
Units courses prerequisite and corequisite
Prerequisite or corequisite units are presented within each program
Learning unit contents
From the laboratory to the pharmacy: legal requirements - part D: introduction to biobanking
We will describe objectives and activities of a biobank including legal, ethic and technical aspects.
Learning outcomes of the learning unit
Prerequisite knowledge and skills
Planned learning activities and teaching methods
Mode of delivery (face to face, distance learning, hybrid learning)
Course materials and recommended or required readings
Work placement(s)
Organisational remarks and main changes to the course
Contacts
From the laboratory to the pharmacy: legal requirements - part D: introduction to biobanking
Stéphanie Gofflot
04/323.2805
stephanie.gofflot@chuliege.be