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12 September 2013 EMEA/CHMP/269452/2008 Assessment report pursuant to Article 30 of Directive 2001/83/EC Targeted and associated names INN of the active substance: teicoplanin Procedure no: EMEA/H/A30/1301
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What is targocid article-30 referral?
Targocid article-30 referral refers to a specific filing requirement related to the medication called Targocid. It is a regulatory process that must be completed in accordance with the guidelines set forth by the relevant authorities.
Who is required to file targocid article-30 referral?
The party responsible for filing the targocid article-30 referral depends on the specific regulations of each jurisdiction. It could be the manufacturer, distributor, or another designated party.
How to fill out targocid article-30 referral?
The process of filling out a targocid article-30 referral involves providing all the necessary information as required by the regulatory authorities. This typically includes detailed product information, safety data, and other relevant documentation. It is important to follow the specific guidelines provided by the authority.
What is the purpose of targocid article-30 referral?
The purpose of targocid article-30 referral is to ensure that the medication Targocid meets all the necessary regulatory requirements for safety and effectiveness, as set forth by the relevant authorities.
What information must be reported on targocid article-30 referral?
The specific information required to be reported on a targocid article-30 referral may vary depending on the jurisdiction. It typically includes details about the medication's composition, manufacturing process, safety data, clinical studies, and other relevant information.
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