Certificates for the illicit manufacture of narcotic drugs and / or psychotropic substances ārsntieciskajām needs approvalThe certificate shall be issued by Latvian citizens and non-citizens and foreigners with residence permits to carry while travelling in the Schengen Agreement count...
The European health insurance cardThe European health insurance card (EHIC) is a document that attests to the right to receive emergency health care, temporary stay in another European Union, Europe...
Registration of the person carrying out mediation dealings with medicinal products (making changes)Intermediation transactions in medicinal products are all activities related to the sale or purchase of medicinal products (excluding wholesale trade of medicinal p...
Changes to the registration documentation for medicinal productsAfter registration of the medicinal product, it may be necessary to introduce changes to the registration documentation of the medicinal product. These may be: - a...
The license holder ikgadējāPārskata II and III of the substances and medicinal products included in and out of the purchase receiptThe licence holder (substances, medicinal products manufacturer; a drug wholesaler) once a year (until 15 February) Report on the State Agency of Medicines shall be...
Quarterly reports on the licence holder included in Registers II and III substances and medicinal products, purchasing, receipt, the submission of the issue of destructionThe licence holder (substances, medicinal products manufacturer; and veterinary medicinal product wholesaler of medicinal products) once a quarter (15 days after th...
Coordination of additional risk mitigation measures included in the drug risk management plan of the Marketing Ownerner1Submission and co-ordination of educational materials specified in the risk management plan of medicinal products to the State Agency of Medicines