Tatiana Dolińska

Tatiana serves as a Senior Clinical Research Scientist at Pure Clinical. She specializes in medical devices, personal protective equipment (PPE), and biocidal products. She has nine years of experience in the medical device sector, focusing on technical documentation and, more recently, clinical investigation procedures. Her responsibilities include reviewing medical device technical documentation and preparing clinical investigation documentation, including Clinical Evaluation Reports (CER), Clinical Investigation Plans (CIP), Investigator’s Brochures (IB), and Clinical Investigation Reports (CIR), in accordance with applicable MDR and GCP requirements and ISO 14155. She holds a PhD and a Master of Science in Engineering degree from the Warsaw University of Life Sciences (SGGW). She gained professional experience at the Office for Registration of Medicinal Products, Medical Devices and Biocidal Products in Poland, as well as at companies involved in the distribution, import, and manufacture of medical devices.

Tatiana Dolińska

Tatiana Dolińska

Clinical Research Scientist

Education (1)

Warsaw University of Life Sciences (SGGW)

PhD, Faculty of Horticulture, Biotechnology and Landscape Architecture

X 2009 – IX 2014

M.Sc, Faculty of Agriculture and Biology

X 2004 – VII 2009

Work Experience (5)

Pure Clinical

Senior Clinical Research Scientist

IX 2026 – Present

Clinical Research Scientist

VI 2024 – VIII 2026

MDR Regulator

Medical Devices Consultant

VIII 2023 – VI 2024

Synoptis Pharma Sp. z o.o.

Expert in Product Registration and Development (Medical Devices)

V 2022 – VII 2023

Specialist in Medical Device Development and Regulation

V 2020 – IV 2022

MEDIF Sp. z o.o.

Registration Specialist (Medical devices)

IX 2017 – IV 2020

The Office for Registration of Medicinal Products

Biocidal Product Senior specialist

VIII 2015 – VIII 2017