Public procurement challengingPublic procurement challenging is a review procedure that allows to carry out a post-control of the legality of the decisions taken by the organisers of procurement...
Authorisation of clinical trials of medicinal products and authorisation of observations on the use of medicinal productsIn order to receive a permit for the commencement of clinical trials of medicinal products and observations of the use of medicinal products, the sponsor or a perso...
Preparation of titrated solutions, indicators and reactive devices for pharmaciesProvision of pharmacies with reagents which are necessary to control the quality of manufactured medicinal products and purified water. In order to receive titrated...
Testing samples of medicinal products for human useUpon the request of the client, the State Agency of Medicines (ZVA) shall perform an expert-examination of samples of medicinal products in order to ascertain the c...
Receiving a product registration status statementThe notification of the status of registration of the product is intended for the representative of the importer of medicinal products participating in internationa...
Assessment of the product documentation on its compliance with the definition of medicinal productsThe manufacturer of the product or his representative shall request an assessment to determine whether the product produced by it complies with the definition of th...
Registration of the manufacturer, distributor and importer of active substances (change)Active substances used for the manufacture or manufacture of medicinal products for human use in a pharmacy must register pharmaceutical activity for the performanc...
Receipt of a product certificateIn order to facilitate the export of medicinal products and to ensure compliance with import requirements in other countries, the State Agency of Medicines shall is...