Excursion to Pharmaceutical Industry - GF153
Title: Exkurze do farmaceutického průmyslu
Guaranteed by: Department of Social and Clinical Pharmacy (16-16220)
Faculty: Faculty of Pharmacy in Hradec Králové
Actual: from 2020
Semester: summer
Points: 0
E-Credits: 1
Examination process: summer s.:
Hours per week, examination: summer s.:0/14, C [HS]
Capacity: unknown / unknown (150)
Min. number of students: unlimited
4EU+: no
Virtual mobility / capacity: no
Key competences:  
State of the course: not taught
Language: Czech
Teaching methods: full-time
Level:  
Explanation: (F,3.r.)
Note: course can be enrolled in outside the study plan
enabled for web enrollment
Guarantor: RNDr. Jana Kotlářová, Ph.D.
Classification: Pharmacy > External Subjects
Examination dates   Schedule   
Annotation -
In this subject is important to acquaint students with function of a pharmaceutical factory. Dduring 1 day long excursion to the pharmaceutical factory students recognize function of a factory, select production, logistic and control processes and Good Manufactoring Practice in the pharmaceutical industry.
Last update: Kotlářová Jana, RNDr., Ph.D. (20.12.2017)
Course completion requirements -

Credit is given for active participation in excursion.

Last update: Kotlářová Jana, RNDr., Ph.D. (20.12.2017)
Literature -

Recommended:

  • http://www.ifpma.org (international federation of pharmaceutical manufactures and associations)

  • http://www.girp.org (The European association of full line wholesalers)

  • web sites - www.who.org; www.fip.org

  • see Reading list from subject Economics and management of pharmaceutical practice

Last update: prepocet_literatura.php (19.09.2024)
Teaching methods -

Excursion.

Last update: Kotlářová Jana, RNDr., Ph.D. (20.12.2017)
Syllabus -

Public information about pharmaceutical factory and their activities, visitation of select parts of factory realised from aspect of principles of Good Manufactoring Practice, production of solid dosage forms, production of semisolid and liquid dosage forms, methods and dokumentation of control of quality of processes, drugs and work in the pharmaceutical industry.

Last update: Kotlářová Jana, RNDr., Ph.D. (20.12.2017)