Scientific Programme

Scientific
Programme


November 6, 2025 -Thursday

18.00-18.20 Welcome
18.20-18.50 Opening Lecture
One Health in the Perspective of a Toxicologist
Félix Carvalho (Portugal)
19.00 Opening Reception

November 7, 2025 -Friday

09.00-09.30 Plenary Lecture
Toxicological Consideration and Risk Assessment of Drug Impurities
Biljana Antoijevic (Serbia)

SESSION 1: Advances in Food Safety and Risk Assessment: Emerging Challenges and Solutions

09.30-10.00 Toxic metals in food and their emerging role as risk factors in hormone-related reproductive cancers
Aleksandra Buha (Serbia)
10.00-10.30 Food Safety Risk Assessment in Türkiye
Serap Hancı (Türkiye)
10.30-11.00 Challenges of the Risk Assessment of Dietary Microplastics
María-Carmen Rubio-Armendáriz (Canary Islands, Spain)
11.00-11.15 Coffee Break

SESSION 2: Epigenetic Mechanisms in Toxicology

11.15-11.45 Epigenetic biomarkers for chemical hazard assessment
Joëlle Rüegg (Sweden)
11.45-12.15 AHR-mediated m6A RNA methylation contributes to PM2.5-induced cardiac defects
Tao Chen (China)
12.15-12.45 Role of epigenetic modifications in the toxicity mechanisms of Fusarium-induced mycotoxins
Ecem Fatma Karaman (Türkiye)
12.45-13.30 Lunch Break

SESSION 3: New Approaches to In Vitro Efficacy/Toxicity Assessment – Advantages and Limitations

13.30-14.00 New air-liquid interface (ALI) system approach for drug efficacy/toxicity testing
Merve Güdül Bacanlı (Türkiye)
14.00-14.30 Challenges in implementing New Approaches Methodologies in the risk assessment of nanomaterials
Ivana Vinković Vrček (Croatia)
14.30-15.00 Organoid models to test drug safety and efficacy
Esra Erdal (Türkiye)
15.00-15.30 Advancements of in vitro methods for inhalation toxicity towards next generation risk assessment
Tommaso Serchi (Luxembourg)

SESSION 4: Cutting-edge Advances in NAMs – What’s New and What’s Next

15.30-15.50 Advancing immunotoxicology: NAMs for immunosuppression and developmental immunotoxicity
Emanuela Corsini (Italy)
15.50-16.10 Advancing ocular safety: insights into the new OECD guideline
Helena Kandarova (Slovakia)
16.10-16.30 NAMs in cosmetics: the future of safety and innovation
Zehra Sarıgöl-Kılıç (USA)
16.30-16.50 Computational and predictive analysis in toxicology
Sanin Haveric (Bosnia and Herzegovina)
16.50-17.15 Coffee Break

SESSION 5: Safety in Psychotropic Medications Treatment

17.15-17.45 Monitoring the safety and tolerability of antipsychotic drug treatment
Christoph Hiemke (Germany)
17.45-18.15 Comprehensive overview on intoxications with psychotropic drugs
Fredrik C. Kugelberg (Sweden)
18.15-18.45 Pharmacokinetic genes variations and response to treatment: the examples of risperidone, aripiprazole and clozapine
Eap-Bin Chin (Switzerland)
18.45-19.15 The impact of pharmacodynamic gene variations on adverse drug reactions in antidepressant treatment
Sinan Süzen (Türkiye)

November 8, 2025 -Saturday

09.00-09.30 Plenary Lecture
Toxicology Risk Management through Interdisciplinary Approaches to Meet ESG Requirements and Sustainability Challenges
Salmaan Hussain B Inayat Hussain (Malaysia)
09.30-09.45 Coffee Break

SESSION 6: The Importance of Genotoxicity Tests in the Biomonitoring of Chemical Hazards in Occupational Settings

09.45-10.10 The comet assay in human biomonitoring
Andrew Collins (Norway)
10.10-10.35 Alkaline Comet and Micronucleus Cytome Assay – The use of the Methods and Their Perspectives through the results of the HCOMET, HUMNAP, EDIAQI, AND BIOMOLTOX Projects
Mirta Milic (Croatia)
10.35-11.00 Steel Industry in Bosnia and Herzegovina – Human Biomonitoring in Exposed Population
Anja Haveric (Bosnia and Herzegovina)
11.00-11.25 Genotoxicity biomarkers in occupational exposure to hazardous compounds in Portugal: Lessons learned on formaldehyde, antineoplastics and volatile organic compounds
Carina Ladeira (Portugal)
11.25-11.50 Occupational exposure to mineral fibers – biomarkers of exposure, effect and susceptibility
Maria Dusinska (Slovakia/Norway)
12.00-13.30 Lunch Break

SESSION 7: Microplastics – State of the Science and the Impacts on Human Health

13.30-13.50 Understanding microplastics and human health concerns
Neslihan Aygun Kocabaş (Belgium)
13.50-14.10 Challenges of microplastics research in risk assessment: Ensuring generation of quality data
Erik Rushton (Netherlands)
14.10-14.30 Plastic chemical additives: determining human risk from microplastic exposure
John Norman (USA)
14.30-14.50 Microplastics: unfolding consequences
Marijana Curcic (Serbia)

SESSION 8: Transporters in Toxicology – Unraveling Mechanisms of Xenobiotic Exposure, Metabolic Dysfunction, and Reproductive Health

15.00-15.40 Fetoplacental toxicity and mycoestrogens at the placental barrier
Lauren M. Aleksunes (USA)
15.40-16.20 Multidrug resistance protein 4 dysfunction drives hepatic steatosis and metabolic dysregulation: Integrated in vivo and in vitro insights
José E. Manautou (USA)
16.20-17.00 Integrating drug development tools to predict per- and polyfluoroalkyl (PFAS)-transporter interactions and disposition to human liver
Angela L. Slitt (USA)
20.00 Gala Dinner

November 9, 2025 -Sunday

09.00-09.30 Plenary Lecture
Mode of action-based refined risk assessment for direct and
indirect genotoxic carcinogens
Andrea Hartwig (Germany)

SESSION 9: Advancements in Understanding the Mechanisms of Organ-Specific Toxicity Induced by Chemicals and Drugs

09.30-10.00 New insight into molecular targets and early key events in genotoxicity and renal carcinogenicity of the mycotoxin ochratoxin A
Johannes Borchers (Germany)
10.00-10.30 Towards understanding the mechanism of methanol-induced optic nerve damage by leveraging human data
Hilmi Orhan (Türkiye)
10.30-11.00 Particle-induced acute phase response as a mechanism-of-action of particle-induced cardiovascular disease
Ulla Vogel (Denmark)
11.00-11.30 Human in vitro models for the detection and understanding of chemical-induced nephrotoxicity
Paul Jennings (The Netherlands)
11.30-11.45 Coffee Break

SESSION 10: European and National Regulation on Medical Devices – Challenges and Opportunities for Toxicologists

11.45-12.15 Medical devices made of substances: challenges on definitions for classification and biosafety assessment
Marco Racchi (Italy)
12.15-12.45 Toxicological challenges for industry in the application of MDR 745/2017
Nina Eriksen (Denmark)
12.45-13.15 Methodological aspects for biosafety compliance in medical devices
Emanuela Testai (Italy)
13.15-13.45 Toxicological risk assessment for extractables/leachables in pharmaceuticals and medical devices
Ahmet Aydın (Türkiye)

12th International Congress of the Turkish Society of Toxicology


PCO

TUNGA TOUR DMC
Kemankeş Karamustafa Paşa Mah.
Gümüş Halka sk. No: 4 Kat: 2-3
34425 – Karaköy /Beyoğlu / Istanbul
registration@tungatour.com
+90 212 243 22 40
+90 532 762 75 95

Secretariat

Prof. Dr. Özlem ATLI EKLİOĞLU
Anadolu University, Faculty of Pharmacy
Department of Toxicology
26210 Tepebaşı/Eskişehir/Turkey
ttdcongress@gmail.com
+90 (222) 335 0580 / 3755

Tunga Tour, 2021