Translated using
Changes in the registration documentation of veterinary medicinal products
Selected Organization: Pārtikas un veterinārais dienests
Brief description:
If it is necessary to make changes to the registration documentation for veterinary medicinal products, the Food and Veterinary Service shall be informed thereof.
Legal persons governed by public law, Private law legal persons
Maximum period (in working days):
The time limit for receiving the service depends on the type of change that you want to make. An expert-examination of the IA type change application shall take 14 days, an expert-examination of the IB type change application - 30 days, an expert-examination of the Type II change application - 60 or 90 days.
Process description
Documents and forms
Other information
Redress options
During a month for the Ministry of Agriculture.

Decisions issued by national authorities in Latvia may be contested, in accordance with the Administrative Procedure Law - In addition to challenging decisions, foreign operators have the possibility to use an alternative dispute settlement mechanism for SOLVIT -
Mock-ups of the labelling of veterinary medicinal products must be approved by the PVD prior to the distribution of such medicinal products in Latvia.
Section 17, Paragraph one of the Pharmaceutical Law states that only medicinal products registered in the Republic of Latvia and included in the Latvian Register of Veterinary Medicinal Products may be distributed in Latvia.
Laws and regulations
Farmācijas likums
(Saeima; likumi; 5/8/1997)
Veterināro zāļu reģistrēšanas kārtība
(Ministru kabinets; noteikumi; 600; 8/11/2006)
Veterināro zāļu izplatīšanas un kontroles noteikumi
(Ministru kabinets; noteikumi; 326; 6/15/2016)
Service references
Pārtikas un veterinārais dienests
Contact details: Pārtikas un veterinārais dienests

Kontaktinformācija: Adrese: Peldu iela 30, Rīga, LV-1050

Tālrunis: 67095230



PVD reģistri -

PVD rekvizīti maksājumu veikšanai -
Information about service restored: 13.10.2020