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Šis dokuments ir veterinārais sertifikāts, kas paredzēts liellopu sugu mājdzīvnieku in vivo iegūto embriju importam, apstiprinot prasības un nosacījumus, saskaņā ar Padomes direktīvu 89/556/EEK.
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What is ANNEX II/ II PIELIKUMS?
ANNEX II/ II PIELIKUMS is a supplementary document required for certain regulatory submissions that details additional information relevant to the application or report.
Who is required to file ANNEX II/ II PIELIKUMS?
Entities such as manufacturers, importers, and distributors that are subject to specific regulatory guidelines must file ANNEX II/ II PIELIKUMS.
How to fill out ANNEX II/ II PIELIKUMS?
To fill out ANNEX II/ II PIELIKUMS, one must accurately provide all requested information, ensuring compliance with guidelines, and double-check for completeness and accuracy before submission.
What is the purpose of ANNEX II/ II PIELIKUMS?
The purpose of ANNEX II/ II PIELIKUMS is to ensure that relevant and necessary information is disclosed to regulatory authorities for evaluating compliance with legal requirements.
What information must be reported on ANNEX II/ II PIELIKUMS?
Information that must be reported on ANNEX II/ II PIELIKUMS includes details about the product, its compliance with safety standards, and any relevant environmental impact assessments.
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