Daten
Offizielle Daten in der Fachveröffentlichung für das folgende akademische Jahr: 2022-2023
Lehrbeauftragte/r
-
Dr. András Tamás FITTLER
associate professor,
Department of Pharmaceutics and University Pharmacy -
Semesterwochenstunden
Vorlesungen: 0
Praktika: 0
Seminare: 28
Insgesamt: 28
Fachangaben
- Kode des Kurses: OTM-QABS-T
- 2 kredit
- Biotechnology BSc
- Specialty Module in Biotechnology modul
- spring
OTV-BMMB-T completed , OTV-IMMU-T completed , OTN-MBFB-T completed
Zahl der Kursteilnehmer für den Kurs:
min. 5 – max. 24
Thematik
Quality assurance and quality management often come to mind in pharmaceutical manufacturing, yet quality can be extended to all things of value. Ensuring the quality of products or services, increases the competitiveness of the organization. Within the framework of the subject, students have the opportunity to get acquainted with the concept of quality, the development of quality management systems and the principles of quality management. The process approach and its significance, as well as the quality loop (PDCA principle) as a basis for quality management thinking. Further, course covers the general aspects of quality management layers, adapting GMP, ISO and external quality assurance in the research, diagnosis and manufacture of biopharmaceutical products. In addition, the course provides the student with a basic understanding of how to integrate these aspects into the latest molecular therapies, molecular diagnostics, and other biotechnology products. Finally, the course provides insight into quality risk management, product recall management, product stability, and end product quality.
Vorlesungen
Praktika
Seminare
- 1. Introduction, development of quality management, GMP and ISO
- 2. Safety first! Personal protective equipment, labelling and waste disposal
- 3. Pharmaceutical and biotech research quality
- 4. Designing quality assurance plan for research
- 5. Constructions, personal quality assurance
- 6. Building standards: using software and lego
- 7. General EU legislative basis
- 8. Quality levels case study, Internal and external environment, and stakeholders
- 9. Quality management in biotech production
- 10. Risk assessment techniques
- 11. Quality Risk Management
- 12. Recalling and processing a product
- 13. Complaint and recall handling
- 14. Testing recalled product and Stability testing
- 15. Product characterization
- 16. Testing impurities
- 17. On-going stability testing
- 18. Nucleic acid analysis
- 19. Biotech products for human use and what to monitor
- 20. Protein analysis
- 21. Biotech products for diagnosis and research
- 22. Monoclonal antibody quality assurance
- 23. Application of the Deming Cycle (Plan-Do-Check-Act)
- 24. Cytotoxic conjugated antibodies quality assurance
- 25. Molecular diagnostics quality
- 26. Molecular diagnostics, biotech or not?
- 27. Final product quality testing
- 28. Final test
Materialien zum Aneignen des Lehrstoffes
Obligatorische Literatur
Vom Institut veröffentlichter Lehrstoff
List of study aids to acquire curriculum (books, notes, other) and all presentations can be downloaded from MS teams and/or Neptun MeetStreet.
Skript
Empfohlene Literatur
Pharmaceutical Manufacturing Handbook (ISBN: 978-0-470-25959-7) chapters: 2.1, 3.1, 3.3, 5.1, 6, 7 .
Handbook: Quality Practices In Basic Biomedical Research (ISBN: 9780198777069) chapters: 1, 2.1.2, 4.3, 4.6.1
Molecular diagnostics chapters: 1 and 2
The Rules Governing Medicinal Products in the European Union EudraLex Chapter 6: Quality Control
https://www.who.int/medicines/areas/quality_safety/quality_assurance/QualityAssurancePharmVol2.pdf
https://www.ema.europa.eu/en/human-regulatory/overview/advanced-therapies/legal-framework-advanced-therapies
Voraussetzung zum Absolvieren des Semesters
Maximum of 25 % absence allowed
Semesteranforderungen
In case of unsuccessful or missed end-of-the term test, a retake opportunity is granted to make up during the last week of the
semester. Assessment of the student performance is carried out according to a ve-grade scale: 100-86,1% -excellent (5); 86-77,1% -good (4); 77- 68,1% -satisfactory (3); 68-60,1% -pass (2); and below 60,0% -fail (1) respectively
Möglichkeiten zur Nachholung der Fehlzeiten
Retake opportunity is possible following personal discussion for the end-of-the term test.
Prüfungsfragen
In-class and inter-class individual assignments, case studies, case discussions must be completed to learn the principles and quality techniques of quality management, and illustrate the biotechnological aspects of quality assurance.
Prüfer
- Dr. Fittler András Tamás
- Elhusseiny Mohamed Mahmoud
Praktika, Seminarleiter/innen
- Dr. Fittler András Tamás
- Elhusseiny Mohamed Mahmoud