Anna Mietelska-Porowska

I have gained new knowledge of the chemical control of production and the regulations governing the introduction of a product into Phase I First-In-Human, and I have expanded and enriched my knowledge of the regulations and principles of planning experiments at non-clinical and preclinical stages of development. I intend to complete the requirements based on the current GLP regulations and guidelines for preclinical and non-clinical phases and implement them in my laboratory, which provides services to perform preclinical studies for small biotechnology companies. Great Lecturers, open to questions and willing to help. A very interesting experience meeting and talking to other participants who are implementing the processes discussed during the course in very different ways. The opportunity to exchange experiences and knowledge was extremely developing.