Az egészségügyi miniszter 21/2009. (VII. 14.) EüM rendelete az emberi alkalmazásra kerülő gyógyszerek forgalomba hozataláról szóló 52/2005. (XI. 18.) EüM rendelet módosításáról

This ministerial decree amends existing regulations concerning the marketing authorisation of medicinal products for human use. It updates the rules governing how drugs are approved and made available to the public. The changes affect pharmaceutical companies seeking to market their products and healthcare professionals involved in drug prescription and dispensing. It ensures continued compliance with national and EU standards.