MLU
PHA.03536.02 - Legal and economical aspects of pharmaceutical biotechnology (Vollständige Modulbeschreibung)
Originalfassung Englisch
PHA.03536.02 5 CP
Modulbezeichnung Legal and economical aspects of pharmaceutical biotechnology
Modulcode PHA.03536.02
Semester der erstmaligen Durchführung
Fachbereich/Institut Institut für Pharmazie
Verwendet in Studiengängen / Semestern
  • Pharmaceutical Biotechnology (MA120 LP) (Master) > Pharmazie Pharmaceut.Biotech.MA120, Akkreditierungsfassung (WS 2008/09 - WS 2015/16) > Pflichtmodule
Modulverantwortliche/r
Weitere verantwortliche Personen
Prof. Dr. P. Imming
Teilnahmevoraussetzungen
Kompetenzziele
• Understanding of drug quality requirements, pre-requisites and activities • Basic knowledge of the European drug quality system • Connection of the European system with international regulations, differences and over-laps • Knowledge of basic concepts for GMP and on differences between European and US regulations • Knowledge of the basic concepts of a) Strategic & business planning (corporate, marketing, financial, R&D) b) value assessment of developmental projects and intellectual properties with simple standard methods (NPV, double-sided NPV, benchmarking etc) c) portfolio strategy d) structuring cooperation agreements e) patent assessment and trading intellectual properties (licensing) f) alliances and joint ventures • Drafting and evaluation of different forms of cooperation agreements • Calculating value of a particular product in development • Understanding and drafting a commercial term sheet for licensing of a particular product from a development to a distributor company • Drafting a business plan
Modulinhalte
Course F.1: Drug quality control - European and international standards and regulations • Requirements for drugs: efficacy, safety, quality • Drug quality: definitions, legal requirements, standards, methods • Good Manufacturing Practices, emphasis on quality; CPMP and ICH guidelines on qual-ity • European, US, and other pharmacopoeiae of international importance
Course F.2: Good Manufacturing Practice - European and international regulations • European GMP regulations • Application of GMP guidelines for biotechnology • Aseptic processing • Qualification of materials and devices for pharmaceutical manufacturing • Process validation • GMP compliant documentation • Qualified persons in GMP manufacturing • Modern concepts for `Quality by Design` and Process Analytical Technology
Course F.3: Economical and marketing aspects, patents and licensing • Strategic planning • Business Plan • Value assessment • Important legal issues for structuring different cooperation agreements • Evaluation of Intellectual Properties • Trading with Intellectual Properties • Exercise Course based on a case study
Lehrveranstaltungsformen Vorlesung (2 SWS)
Vorlesung (1 SWS)
Vorlesung (1 SWS)
Kursus
Unterrichtsprachen Deutsch, Englisch
Dauer in Semestern 1 Semester Semester
Angebotsrhythmus Modul jedes Sommersemester
Aufnahmekapazität Modul unbegrenzt
Prüfungsebene
Credit-Points 5 CP
Modulabschlussnote LV 1: %; LV 2: %; LV 3: %; LV 4: %.
Faktor der Modulnote für die Endnote des Studiengangs 1
Modulveran­staltung Lehrveranstaltungs­form Veranstaltungs­titel SWS Workload Präsenz Workload Vor- / Nach­bereitung Workload selbstge­staltete Arbeit Workload Prüfung incl. Vorbereitung Workload Summe
LV 1 Vorlesung Economical and marketing aspects, patents and licensing 2 0
LV 2 Vorlesung Drug quality control - European and international standards and regulations 1 0
LV 3 Vorlesung Good manufacturing practice - European and international regulations 1 0
LV 4 Kursus Selbststudium 0
Workload modulbezogen 150 150
Workload Modul insgesamt 150
Prüfung Prüfungsvorleistung Prüfungsform
LV 1
LV 2
LV 3
LV 4
Gesamtmodul
Klausur
Wiederholungsprüfung
Regularien Teilnahme­voraussetzungen Angebots­rhythmus Anwesenheits­pflicht Gewicht an Modulnote in %
LV 1 Sommersemester Nein %
LV 2 Sommersemester Nein %
LV 3 Sommersemester Nein %
LV 4 Sommersemester Nein %