Μ3. Preclinical and clinical drug evaluation

Purpose/Objectives of the Course

The following thematic units are developed in the course: Pharmacological evaluation and applications. Drug delivery and pharmacogenomics approach. Introduction to Biopharmaceutics. Biopharmaceutical Classification System, Determination of biopharmaceutical properties, Active ingredient release profile from tablets/capsules. Dissolution rate control. Bioavailability and basic pharmacokinetics. Design, – Biowaiver Justification. Bioequivalence and IVIVC studies. Ethical evaluation, preparation, organization, implementation and monitoring of experimental protocols.  Good Clinical Practice (GCP).

Coordinator

Teachers

Teaching Assistants

Course Organization​

ECTS: 8

Lectures: 8
PC application: 3

Workload

200 – 240 hours
Lectures/Workshops: 70 hours
Personal effort: 130 hours

Course Lectures

Week

Faculty

Teaching method 

Description of teaching unit

1

Kahrimanis Kyriakos.

Prof. of Pharm. Technology, AUTH

Theory

Biopharmaceuticals, Biopharmaceutical Classification System

Determination of biopharmaceutical properties

2

Barbalexis Panagiotis

Asst. Prof. of Pharm. Technology, AUTH

Theory

Bioavailability and basic pharmacokinetics

3

Barbalexis Panagiotis

Asst. Prof. of Pharm. Technology, AUTH

Theory

Bioequivalence studies and IVIVC

4

Vizirianakis Ioannis, Asst. Professor of Pharmacology AUTH

Theory

Development of new drugs A: Pharmacological evaluation and applications

5

Vizirianakis Ioannis, Asst. Professor of Pharmacology AUTH

Theory

New Drug Development B: Drug Delivery and Pharmacogenomics Approach

6

Vizirianakis Ioannis, Asst. Professor of Pharmacology AUTH

 

Mystridis Georgios MSc, PhD candidate: licensed to use the Simcyp platform

P/C application

Application of population pharmacokinetic models through the Simcyp platform in pharmaceutical research. Development of new drugs (part I)

7

Vizirianakis Ioannis, Asst. Professor of Pharmacology AUTH

 

Mystridis Georgios MSc, PhD candidate: licensed to use the Simcyp platform

P/C application

Application of population pharmacokinetic models through the Simcyp platform in pharmaceutical research. Development of new drugs (part II)

8

Georgios Patrinos, Prof. of Pharmacogenomics and Pharmaceutical Biotechnology, Univ. Patras

Theory

Pharmacogenomics in the post-genomic era

9

Paspaltzis Ioannis MSc, PhD Pharmacology, EDIP, AUTH

Theory

Introductory concepts in biotechnology

10

Papadopoulou Lefkothea

Professor of Pharmacology AUTH

Theory

“Pharmaceutical Biotechnology: Application of Protein Transduction Technology (PTD Technology) for the production of recombinant proteins in the context of therapeutic approach to monogenic-metabolic diseases Part I

11

Papadopoulou Lefkothea

Professor of Pharmacology AUTH

Theory

“Pharmaceutical Biotechnology: Application of Protein Transduction Technology (PTD Technology) for the production of recombinant proteins in the context of therapeutic approach to monogenic-metabolic diseases Part IΙ

12

Papadopoulou Lefkothea

Professor of Pharmacology AUTH

Lab

Antimicrobial chemotherapeutic drugs: method for determining the sensitivity and resistance of microorganisms to antibiotics (Antibiogram)

13

 

Kafkala Stella, MSc, cPhD, Analytical Development Director, Genepharm

Theory

API release profile from tablets/capsules

14

Exams/Theory

Examination of the course

Final exam

0%

Course Essays

0%

Related Bibliography

PHARMACEUTICAL TECHNOLOGY, AULTON, DRUG DESIGN AND MANUFACTURE (4TH ED.)

Author: MICHAEL E. AULTON , KEVIN M.G. TAYLOR

Edited by: KYRIAKOS KACHRIMANIS, IOANNIS NIKOLAKAKIS

ISBN: 9789605832162

Link

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