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NMVO ITALIA

Official communication to Marketing Authorization Holders, On-Boarding Partners and Parallel Importers

Following a notification from the EMVO (European Medicines Verification Organization) regarding the upload into the system of several batches labeled as "TEST", all Marketing Authorization Holders, On-Boarding Partners, and Parallel Importers are reminded that, for any ๐ญ๐ž๐ฌ๐ญ activity related to data uploads for the Italian market, it is mandatory to exclusively use the ๐๐ž๐๐ข๐œ๐š๐ญ๐ž๐ ๐ˆ๐๐„ (๐๐ฎ๐š๐ฅ๐ข๐ญ๐ฒ) ๐ž๐ง๐ฏ๐ข๐ซ๐จ๐ง๐ฆ๐ž๐ง๐ญ ๐จ๐Ÿ ๐ญ๐ก๐ž ๐„๐ฎ๐ซ๐จ๐ฉ๐ž๐š๐ง ๐‡๐ฎ๐›. The IQE environment has been specifically designed to support testing phases in complete safety.

Running tests in the Production (PROD) environment carries a serious risk of compromising the integrity of the overall data within the Italian system.

All involved parties are hereby requested to ensure that all ๐ญ๐ž๐ฌ๐ญ๐ข๐ง๐  ๐š๐œ๐ญ๐ข๐ฏ๐ข๐ญ๐ข๐ž๐ฌ ๐š๐ซ๐ž ๐ฉ๐ž๐ซ๐Ÿ๐จ๐ซ๐ฆ๐ž๐ ๐ž๐ฑ๐œ๐ฅ๐ฎ๐ฌ๐ข๐ฏ๐ž๐ฅ๐ฒ ๐ฐ๐ข๐ญ๐ก๐ข๐ง ๐ญ๐ก๐ž ๐ˆ๐๐„ ๐ž๐ง๐ฏ๐ข๐ซ๐จ๐ง๐ฆ๐ž๐ง๐ญ.

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