SubjectsSubjects(version: 945)
Course, academic year 2023/2024
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Development of Pharmaceutical Products - GF379
Title: Vývoj léčivého přípravku
Guaranteed by: Department of Pharmaceutical Technology (16-16210)
Faculty: Faculty of Pharmacy in Hradec Králové
Actual: from 2022
Semester: winter
Points: 0
E-Credits: 4
Examination process: winter s.:written
Hours per week, examination: winter s.:0/32, C+Ex [HS]
Capacity: unknown / unlimited (20)
Min. number of students: unlimited
4EU+: no
Virtual mobility / capacity: no
Key competences:  
State of the course: taught
Language: Czech
Teaching methods: full-time
Teaching methods: full-time
Level:  
Note: course can be enrolled in outside the study plan
enabled for web enrollment
Guarantor: doc. PharmDr. Zdeňka Šklubalová, Ph.D.
Co-requisite : GF346
Interchangeability : GF288
Is interchangeable with: GF320
Annotation -
Last update: doc. PharmDr. Zdeňka Šklubalová, Ph.D. (04.12.2021)
The subject is related to the subject Pharmaceutical Technology 1 and 2 and deals to the students who would like to enlarge their knowledge in Pharmaceutical Technology, particularly in the development and formulation of the pharmaceutical preparation including choice of active substance, dosage form, excipients and final evaluation of the product. The subject belongs to Area of Specialization in Pharmaceutical Technology The capacity limit: 5
Course completion requirements -
Last update: doc. PharmDr. Zdeňka Šklubalová, Ph.D. (04.12.2021)

The subject is concluded by passing the written exam.

100% presence in lectures/seminars is required.

Literature -
Last update: doc. PharmDr. Zdeňka Šklubalová, Ph.D. (04.12.2021)

Obligatory:

  • . . In Allen, Loyd V. (ed.). Remington : an introduction to pharmacy . London: Pharmaceutical Press, 2013, s. -. ISBN 978-0-85711-104-3..
  • . . In Allen, Loyd V.. Pharmaceutical dosage forms and drug delivery systems . Philadelphia: Wolters Kluwer, 2018, s. -. ISBN 978-1-4963-7291-8..
  • . . In Gad, Shayne C., (ed.). Pharmaceutical manufacturing handbook : production and processes . Hoboken, N.J.: John Wiley & Sons, 2008, s. -. ISBN 978-0-470-25958-0..
  • . . In Swarbrick, James, (ed.). Encyclopedia of pharmaceutical technology . New York: Informa Healthcare, 2007, s. -. ISBN 0-8493-9399-X..

Syllabus -
Last update: doc. PharmDr. Zdeňka Šklubalová, Ph.D. (04.12.2021)

Syllabus

·      Development process and phases

·      Characterization of API

·      Development of analytical methods, dissolution studies

·      Formulation process, scale-up

·      Development of solid dosage form

·      Modified release

·      Evaluation of the product, bioequivalency

Learning resources -
Last update: doc. PharmDr. Zdeňka Šklubalová, Ph.D. (04.12.2021)
Department of Pharmaceutical Technology | Intranet FAF (cuni.cz)
Teaching methods -
Last update: doc. PharmDr. Zdeňka Šklubalová, Ph.D. (04.12.2021)

Seminars and lectures

The subject is supported by teachers from Zentiva.

Requirements to the exam -
Last update: doc. PharmDr. Zdeňka Šklubalová, Ph.D. (04.12.2021)

The subject is concluded by passing the written exam. 75 % is necessary to pass.

100% presence in lectures/seminars is required.

 
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