Zákon č. 378/2007 Sb., o léčivech a o změnách některých souvisejících zákonů (zákon o léčivech)

This Czech law regulates medicinal products, including their manufacturing, distribution, and use. It aims to ensure the quality, safety, and efficacy of medicines available to the public. The act affects pharmaceutical companies, healthcare providers, and patients by setting standards for medicines and related activities within the Czech Republic.