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<oembed><version>1.0</version><provider_name>European Industrial Pharmacists Group (EIPG)</provider_name><provider_url>https://eipg.eu</provider_url><title>EIPG Feedback on Revised Annex 1 - European Industrial Pharmacists Group (EIPG)</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content"&gt;&lt;a href="https://eipg.eu/eipg-feedback-annex-1/"&gt;EIPG Feedback on Revised Annex 1&lt;/a&gt;&lt;/blockquote&gt;
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&lt;/script&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://eipg.eu/eipg-feedback-annex-1/embed/" width="600" height="338" title="&#x201C;EIPG Feedback on Revised Annex 1&#x201D; &#x2014; European Industrial Pharmacists Group (EIPG)" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;</html><thumbnail_url>https://eipg.eu/wp-content/uploads/2013/10/eipg-thumb-6.jpg</thumbnail_url><thumbnail_width>400</thumbnail_width><thumbnail_height>285</thumbnail_height><description>The European Commission recently launched a targeted stakeholders consultation on the revision of Annex 1, on manufacturing of sterile medicinal products, of the Eudralex Volume 4. EIPG has reviewed the document and, following feedback from its members, has submitted its comments to the EMA. Read the EIPG Comments on the revised Annex 1.</description></oembed>
