Περιγραφή:
a) Preformulation tests and selection of excipients and dosage form.
b) Characterization of raw materials for the production of dosage forms.
c) Principles, mechanisms, and variables affecting the quality of the end products during pharmaceutical unit operations.
d) Specific formulation aspects of solid dosage forms (powders, capsules, tablets, pellets, inhalations).
e) Design, development and production of liquid dosage forms.
f) Production of sterile dosage forms.
g) Industrial Pharmaceutical Microbiology.
h) Controlled (programmed release) dosage forms. Recent research and development trends in pharmaceutical formulation.
i) Production of biotechnological pharmaceutical materials (peptides and proteins). Preformulation stages, selection of the dosage forms and the excipients involved. Stability assessment and prediction of the biotechnological products.
ECTS: 10
Ώρες Διδασκαλίας: 3
Εξάμηνο: 1
Περιγραφή Μαθήματος κατά ΜΟΔΙΠ: http://qa.auth.gr/en/class/1/180005401
Description:
a) Preformulation tests and selection of excipients and dosage form.
b) Characterization of raw materials for the production of dosage forms.
c) Principles, mechanisms, and variables affecting the quality of the end products during pharmaceutical unit operations.
d) Specific formulation aspects of solid dosage forms (powders, capsules, tablets, pellets, inhalations).
e) Design, development and production of liquid dosage forms.
f) Production of sterile dosage forms.
g) Industrial Pharmaceutical Microbiology.
h) Controlled (programmed release) dosage forms. Recent research and development trends in pharmaceutical formulation.
i) Production of biotechnological pharmaceutical materials (peptides and proteins). Preformulation stages, selection of the dosage forms and the excipients involved. Stability assessment and prediction of the biotechnological products.
ECTS: 10
Hours: 3
Semester: 1
Description MODIP: http://qa.auth.gr/en/class/1/180005401