Tag: EAEU

Published Amendments to the EAEU Veterinary Drugs Circulation Rules: The Transition Period has been Extended until 2030

On March 25, the text of EEC Council Decision No. 33 of February 24, 2026, was officially published. It...

Rosselkhoznadzor has received authority to issue veterinary EAEU GMP certificates

In Russia, the legal framework for issuing EAEU GMP certificates to veterinary medicine manufacturers has been finalized. The Russian...

What Happens in 2031? Regulator Sets “Deadline” for EAEU Veterinary Drug Rules

Since March 2024, supranational rules for the circulation of veterinary medicinal products have been officially in effect within the...

Transparency as an Advantage: AstraZeneca Proposes Unifying EAEU Clinical Trial Databases

Creating a unified digital ecosystem for clinical trials (CT) can turn data transparency into a key competitiveness factor for...

Transition to EAEU Standards: GMP Certification Rules for Veterinary Drugs are Changing

A draft Decree of the Government of the Russian Federation updating the regulatory framework in the field of veterinary...

Important changes in the conduct of pharmaceutical inspections of veterinary manufacturers in accordance with the EAEU Rules

At the end of last year, the third version of the draft amendments to the EEC Council Decision of...

The Mathematics of Sovereignty: EEC Approves Points-Based Procurement System for Pharma

On January 1, 2026, the pharmaceutical market of the Eurasian Economic Union (EAEU) shifted to a fundamentally new model...

The EAEU has established uniform rules for the circulation of veterinary drugs

The Council of the Eurasian Economic Commission (EEC) approved new rules on regulation of veterinary drugs circulation in the...

Transition of Veterinary Manufacturers to the EAEU GMP Rules

In October 2020, the Federal Service for Veterinary and Phytosanitary Surveillance (Rosselkhoznadzor) announced that from January 1, 2021, the...