PharmExpert: Analytical Practices for the Pharmaceutical Industry: Roadmap and Implementation
Dates
Past dates: June 2024
Format
Online
Course Objectives
The course provides a roadmap for analytical work in pharmaceutical R&D and quality control laboratories, covering analytical method development, optimization of existing methods, analytical method transfer in industry, analytical validation, analytical challenges, impurity testing and the toxicological assessment of pharmaceutical impurities.
Who Can Attend
- Pharmacists
- Chemists
- Chemical engineers
- Pharmacy students
- Chemistry students
- Chemical engineering students
Course Content
- Developing an analytical method for a new molecule
- Optimizing an existing analytical method
- Analytical method transfer in industry
- Full analytical validation: Practical exercises using sample data
- Analytical challenges illustrated through examples from the pharmaceutical industry
- Impurity testing and quality control testing
- Toxicological assessment of pharmaceutical impurities
Duration and Capacity
Duration: 10 hours (2 hours each on Tuesday and Thursday, 6 hours on Saturday)
Capacity: 50 participants
Course Coordinator
- Prof. Dr. Halil İbrahim Ulusoy
- Assoc. Prof. Dr. Songül Ulusoy
- Prof. Dr. Belma Gümüşel
Instructors
- Prof. Dr. Halil İbrahim Ulusoy
- Assoc. Prof. Dr. Songül Ulusoy
- Prof. Dr. Belma Gümüşel