• TOWER: power line and tower modeling, control, modification, and reinforcement• Implementation of TOWER models into PLS-CADD

Sample preparation for transmission electron microscopy (TEM): chemical or cryofixation, dehydration, resin embedding, ultramicrotomy, negative and positive staining;Sample preparation for scanning electron microscopy (SEM): fixation, dehydration, critical point drying, coating with conductive material;Obtaining images in TEM and SEM

Department Institute of Experimental Toxicology and Medical andBiological TestsHistological examination of tissues of target organs as a part of pre-clinical toxicological studies of chemical substances and pharmaceuticals in compliance with the GLP-standards, OECD 408, 451, 452, 453, 443 (subchronic, chronic and reproductive studies), applicable regulatory requirements, SOPs;Statistical analysis of the obtained data; Writing of SOPs, updating SOPs according to requirements OECD; Writing of Study Protocols and Study Reports, submission to the Regulatory Authority; Ensuring that the quality control procedures are implemented during every step of the study;CAPA handling;Participating to the risk management process;Ensuring the availability of required tools, including calibrated measuring equipment; Expert activity in Regulatory Toxicology field: analysis Dossier of toxicological studies, toxicological assessment of chemicals; Scientific activity: writing of articles, participation in medical scientific events (conferences, congresses etc.).

Department Conformity Assessment Body «Ecohyntox» (UA.TR.118)Conformity assessment of different classes of medical devices according toTechnical Regulations for medical devices No. 753, medical devices for in vitrodiagnostics No. 754 and active implantable medical devices No. 755 (based onrequirements of MDD, IVDD and AIMDD);Toxicological examination of medical devices according to subsections of ISO10993 «Biologicalevaluation of medical devices»;Certification of management systems to requirements of DSTU EN ISO9001:2018 (EN ISO 9001:2015, IDT; ISO 9001:2015, IDT) «Quality managementsystems. Requirements»; DSTU EN ISO 13485:2018 (EN ISO 13485:2016, IDT;ISO 13485:2016, IDT) «Medical devices. Quality management systems.Requirements for regulatory purposes»;Participating in internal and external audits;CAPA handling and PMS (complaints, vigilance and Reporting);Participating to the risk management process;Liaising with the local KOLs;Writing of Study Protocols, Study Reports, Certificates of Conformity.

Department of complex toxicological and hygienic assessment ofmedical devices, cosmetics products and consumer goodsPlanning and implementation of pre-clinical toxicological studies (medical devices, nutraceuticals, and supplements) in compliance with GLP and OECD standards, contributing scientific and operational expertise;Writing and updating SOPs, as well as Study Protocols and Study Reports, ensuring alignment with regulatory requirements;Coordination with cross-functional teams to ensure study compliance and quality control throughout the research process;Internal and external audits for maintaining compliance with CAPA handling and risk management;Scientific activity: writing of articles, participation in medical scientific events(conferences, congresses and others).

Department of Hygiene and Toxicological-Hygienic Examination of Foodand Consumer Goods, Sector for Laboratory Research of Alcohol and TobaccoProducts.Toxicological examination of Food, Consumer Goods, alcohol and tobaccoproducts;Writing of Study Protocols, Study Reports;Issuance of permit documentation of sanitary-epidemiological examination forapproval by the RegulatoryAuthority