Δομή Προγράμματος

Section: A – Compulsory Courses

• Drug Discovery and Development (7,5 ECTS)
• The DRA Professional (7,5 ECTS)
• EU Regulatory Affairs System (7,5 ECTS)
• Pharmaceutical Industry Ethics (7,5 ECTS)
• Regulatory Strategy and Marketing Applications for new (7,5 ECTS)
• Drugs (7,5 ECTS)
• Clinical Trials: Issues in Design, Conducts and Evaluation (7,5 ECTS)
• International Regulations (ICH & FDA) (7,5 ECTS)
• Preclinical and Clinical Development and Documentation (7,5 ECTS)
• Health Technology Assessment (7,5 ECTS)

Section: B – Elective Courses

• Product’s Life Cycle Activities (7,5 ECTS)
• Regulation of Herbal Medicinal Products (7,5 ECTS)
• Regulation of Medical Devices (7,5 ECTS)
• Pharmaceutical Industry Ethics (7,5 ECTS)

Section: C – Postgraduate Assignment

• Post Graduate Assignment (15 ECTS)
   

Μαθήματα ανά Εξάμηνο

Semester 1

• Drug Discovery and Development (7,5 ECTS)
• The DRA Professional (7,5 ECTS)
• EU Regulatory Affairs System (7,5 ECTS)
• Pharmaceutical Industry Ethics (7,5 ECTS)

Semester 2

• Regulatory Strategy and Marketing Applications for new Drugs (7,5 ECTS)
• Clinical Trials: Issues in Design, Conducts and Evaluation (7,5 ECTS)
• International Regulations (ICH & FDA) (7,5 ECTS)
• Preclinical and Clinical Development and Documentation (7,5 ECTS)

Semester 3

• Product’s Life Cycle Activities (7,5 ECTS)
• Pharmacovigilance and Pharmacoepidemiology (7,5 ECTS)
• Post Graduate Assignment (15 ECTS)

Το πιο πάνω πρόγραμμα ανά εξάμηνο είναι ενδεικτικό. Μερικά από τα μαθήματα είναι επιλογής και μπορούν να αντικατασταθούν με άλλα.