On 27 December 2019, seminar titled “Medical Device Biocompatibility and Clinical Evaluation Training With Medical Device Regulation (MEDR) Perspective” was organized by Istanbul Chamber of Industry. At the seminar, the Vice Rector of our university and Head of the Toxicology Department Prof. Dr. Ahmet Aydın, our Vice Dean and Pharmaceutical Toxicology Department Academic Member Assoc. Dr. Hande Sipahi, Pharmaceutical Toxicology Faculty Member Assoc. Dr. Muhammed Hamitoğlu and Head of the Pharmacology Department Prof. Dr. Turgay Çelik took place as a speaker.

Schedule of the Training

09:00 - 09:30  Registration and Opening
09:30 - 10:15  Definition and classification of medical devices (Prof. Dr. Ahmet Aydın)
10:15 - 11:00  Test Methods to Choose for Medical Devices (Prof. Dr. Ahmet Aydın)
11:00 - 11:15  Coffee Break
11:15 - 12:00  ISO 10993 Test Methods and Brief Explanations-I (Assoc. Prof. Hande Sipahi)
12:00 - 12:45  ISO 10993 Test Methods and Brief Explanations- II (Assoc. Prof. Muhammed Hamitoğlu)
12:45 - 14:00  Lunch Break
14:00 - 14:45  Sample Selection Criterias (Assoc. Prof. Hande Sipahi & Assoc. Prof. Muhammed Hamitoğlu)
14:45 - 15:30  Biocompatibility Assessment Criteria and Reporting (Prof. Dr. Ahmet Aydın)
15:30 - 15:45  Coffee Break
15:45 - 16.30  Clinical Research of Medical Devices (Prof. Dr. Turgay Çelik)
16:30 - 17.00  Discussion and Evaluation

The Vice Rector of our university and Head of the Toxicology Department Prof. Dr. Ahmet Aydın giving his speech

Our Vice Dean and Pharmaceutical Toxicology Department Academic Member Assoc. Dr. Hande Sipahi giving her speech

Pharmaceutical Toxicology Faculty Member Assoc. Dr. Muhammed Hamitoğlu giving his speech

Head of the Pharmacology Department Prof. Dr. Turgay Çelik giving his speech

Photoshoot with our lecturers after the seminar