The government approved the rules for submitting to the Rosselkhoznadzor documents on veterinary drugs put into circulation

If the drug is produced in RUSSIA for the first time, you will additionally need to provide the protocols of tests of the first two batches carried out in an accredited testing laboratory.

In addition, manufacturers or importers of veterinary drugs annually, no later than February 1, are required to submit to the ROSSELKHOZNADZOR a test report conducted in an accredited laboratory for one batch of each trade name of the drug that entered civil circulation during the year.

Entering into civilian circulation immunobiological preparations, such as vaccines or sera, will be possible only on the basis of a permit obtained from Rosselkhoznadzor. Permission will be issued based on the results of tests of the first two batches of the drug in an accredited testing laboratory.

The new rules will come into force on September 1, 2023 and will be valid until September 1, 2029. Items relating to the procedure for issuing permits for the introduction of immunobiological preparations into civil circulation will come into force on March 1, 2024.