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Ankara, TR · Germantown, MD, US — Pharma · Medical · Cosmetic · Food supplement

PharmExpert: Strategic Module 3: Solid and Semi-solid Dosage Forms and Pharmaceutical Development

Dates

Past dates: 8–11 April 2026

Format

Online

Course Objectives

Organized by Mentor Ar-Ge Academy, this course aims to help professionals working in pharmaceutical regulatory affairs and students planning a career in this field strengthen their foundational and critical knowledge of semi-solid and solid dosage forms covered in Module 3.

Who Can Attend

  • Pharmacists
  • Physicians
  • Graduates in biology, chemistry and chemical engineering
  • 5th-year pharmacy students
  • Final-year students in biology, chemistry and chemical engineering

Course Content

Day 1: Wednesday, 8 April

20:00–20:10 Opening

20:10–21:10 Sections of Module 3 and the Scope of Drug Product (3.2.P) — CTD – Sections of Module 3 · The technical role of Section 3.2.P (Drug Product) in a marketing authorization application · Principles for documenting pharmaceutical development in accordance with ICH Q8

21:10–22:10 Advanced CTD/Module 3 Training for Solid Dosage Forms — Solid Dosage Forms and Their Defining Characteristics

in Relation to Section 3.2.P

22:10–23:10 Quality Target Product Profile for Solid Dosage Forms · Critical Quality Attributes of Solid Dosage Forms

Day 2: Friday, 10 April

20:00–22:00 Advanced CTD/Module 3 Training for Solid Dosage Forms — Examining Critical Issues in Preparing Section 3.2.P

Using a Hypothetical Solid Dosage Form Formulation

Day 3: Saturday, 11 April

10:00–11:00 Advanced CTD/Module 3 Training for Semi-solid Dosage Forms — Semi-solid Dosage Forms and Their Defining Characteristics in Relation to Section 3.2.P

11:00–12:00 Methodology and Evaluation of Selected Critical Tests for Semi-solid Dosage Forms

12:00–13:00 Lunch Break

13:00–14:00 Advanced CTD/Module 3 Training for Semi-solid Dosage Forms — Quality

Target Product Profile for Semi-solid Dosage Forms · Critical Quality Attributes of Semi-solid Dosage Forms

14:00–15:00 Preparing Section 3.2.P Using a Hypothetical Semi-solid Dosage Form Formulation:

Examining Critical Issues

15:00–16:00 Questions and Answers, and Closing

Duration and Capacity

Duration: 10 hours

Capacity: 40 participants

Course Coordinator

Contact us for details.

Instructors

  • Prof. Dr. Sibel Bozdağ Pehlivan