D.9. Key Learning Outcomes

1. Learns preformulation and formulation studies, effect of physicopharmaceutical properties on the release properties of the active ingredients and has advanced knowledge on bioavailability and bioequivalence of formulations.

2. Obtains sufficient knowledge about industrial production, quality control, quality assurance systems, the guidelines such as GMP, GLP, GCP, NDA, ANDA, BA/BE, QA/QC and bioanalytical method validation and preparation of new drug application files.

3. Learns preparing application files for animal/human experiments, and the procedures to apply for permission from ethical committees.

4. Contributes to national and international scientific projects as researcher or supervisor, may use literature data, may generate original projects, suitable methods.

5. Gains lifelong learning characteristics according to the ethical issues.

6. Has advanced knowledge on statistical methods.

7. Follows and evaluates the current updated knowledge in Biopharmaceutics and Pharmacokinetics, finds new and original methods, learns how to use laboratory equipment, improves the current state of knowledge, and publishes the results in national and international journals.

8. Has enough knowledge to direct scientific discussions in different groups.

9. Follows the current improvements in their area and apply these current improvements in their studies and use them for the benefit of the public.

10. Knows the ethical rules in scientific and cultural fields; and uses these rules for the solution of the problems.

11. Gains the characteristics of generative and critical thinking.