||The service will allow a natural person or a legal entity to report on the treatment of active substances within the scope of production, distribution, import in accordance with Section 12a of Act no. No. 362/2011 Coll. On Medicinal Products and Medical Devices, as amended. The relevant information can be provided via the form available on the ŠKL website in paper form, as well as fully electronically through the form published on the Central portal of the public administration (slovakia.sk). For electronic submission to slovakia.sk, it is necessary to use eID (Electronic Citizenship Card) and KEP (Qualified Electronic Signature).