Andreina Pietzka, Ch. Ing., has worked in the health science sector for over seven years. Since 2022, she has supported global clients as a QA/RA expert at qtec, focusing on regulatory compliance and product approvals for both medical devices and IVDs.
As a trainer at the qtec Academy, she teaches regulatory topics including MDR, technical documentation, product approval strategies, and project management tools such as Gantt charts and Kanban boards.
What matters most to her as a speaker: "Beyond theory, I strive to help participants truly understand the requirements and how to implement them practically. Every product is different—even if the regulations are the same, there are often multiple paths to meet them effectively. My goal is to support our clients in the successful development and registration of their products."
