№ lp_1_2_46115
Guide for users on how to accurately record suspected adverse event reports in the EU veterinary pharmacovigilance database, including identification numbers, reporting fields, follow-ups, and compliance with VICH standards.
Year: 2023
Document Number: EMA/371192/2021 – Rev.12
Division: Veterinary Medicines Division
Subject: Pharmacovigilance, Adverse Event Reporting
Type: Guidance document
Intended Audience: Registered user organisations and individual EVWEB/Gateway users
Scope: EU Union veterinary pharmacovigilance database EudraVigilance Veterinary (EVV)
Date Issued: 11 July 2023
References: VICH GL42, VICH GL30, VICH GL35, EVWEB User Manual, EU VICH adverse event report implementation guide
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.

Don’t have cryptocurrency yet?

You can still complete your purchase in a few minutes:
  1. Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
  2. In the app, tap Send.
  3. Select network, paste our wallet address.
  4. Send the exact amount shown above.
After sending, paste your TXID (transaction ID) and your email to receive the download link. Need help? Contact support and we’ll guide you step by step.