For 7 years now, I have been constantly delved into this fascinating field. The texts I usually deal with concern: EMA documents (SPCs, PILs, EPARs, in general any human or veterinary regulatory document), scientific papers, medical devices materials, clinical trials, patents, medical reports, e-Learning courses, questionnaires, Informed Consent Forms. By completing a designated postgraduate master's degree, I acquired the necessary tools to deal with this particular type of documents.