Vigilance reports

Drug/vaccine side effects (in Latvian)

Pharmacovigilance reports of residents or medical practitioners and pharmacists - reporting of side effects of medicinal products.

Biovigilance reports (in Latvian)

Vigilance reports relating to human blood, tissues, cells and organs.

Incident reporting for medical devices (in Latvian)

Warnings of a medical treatment institution regarding an incident related to a medical device.

Medicinal Product Register of Latvia

Medicinal Product Register of Latvia

Medicinal products included in the Register of Medicinal Products of the Republic of Latvia, as well as medicinal products centrally registered and parallel imported into the European Union, their availability, instructions for use and other information.

Shortages of medicines

Information on medicinal products reported by the Marketing Authorisation Holder as a result of the shortage of supply.

Report on medicine shortage

Let us know about non-accessible medicinal products – for citizens, pharmacies, hospitals, marketing authorisation holders.

Marketing authorisation, renewal, withdrawal of marketing authorisation

Information regarding marketing authorisation, renewal, withdrawal of marketing authorisation in the Latvian Register of Medicinal Products.

Variations of the marketing authorisations

Information on approved, refused or partially approved changes in the registration dossier of the medicinal product.

Active substances

Active substances in Latvian, English and Latin.

ATC classification

Anatomically therapeutic chemical code classification in Latvian and English.

Conclusion on the therapeutic and cost effectiveness of medicines (in Latvian)

Submissions for the receipt of the conclusion on the therapeutic and cost effectiveness of medicinal products.

Notification for the Agency about the beginning of distribution of medicinal products intended for the market of another EU/EEA country in the Republic of Latvia

For marketing authorisation holders (or their local representatives) to notify the Agency about the beginning of distribution of medicinal products intended for the market of another EU/EEA country in the Republic of Latvia.

List of export restrictions

A list of medicinal products in respect of which the National Health Service and the marketing authorisation holder of medicinal products or a wholesaler of medicinal products has entered into a contract regarding financial participation and the export of which to the European Union Member States or export is permitted only after receipt of the authorisation of the State Agency of Medicines.

Decisions made by the Agency regarding non-application of Sunset Clause

About exemptions granted from Sub-paragraphs 125.1 and 125.2 of Cabinet Regulation No 376 of the Republic of Latvia of 9 May 2006 „Procedures for the Registration of Medicinal Products”

Medicinal products for whom distribution in another EU/EEA packaging was approved

List of medicinal products for whom the Agency has received notifications from marketing authorisation holders on the basis of points 6.3 and 7.6 of Regulation No 57 or for which the Agency has authorised the distribution of medicinal products in packaging intended for the market of another country.
The data has been published on the list since January 1, 2024.

Pharmaceutical companies

LPC registry

Pharmacies, wholesalers, producers, manufacturers of active pharmaceutical substances registered in Latvia and EU/EEA licences

Map of pharmacies (in Latvian)

Information to the public regarding the location of pharmacies and services provided.

LPC submissions and decisions (in Latvian)

Submissions received and decisions taken.

Medical technologies

Medical Technology Database (in Latvian)

Database of medical technology used in medical treatment.

Approval, supplementation, withdrawal of MT (in Latvian)

Submissions for approval, supplementation and withdrawal of new medical technologies (MT).