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    <title>APPLICATION FOR CERTIFICATION OF EXPORT PERFORMANCE OF UNITS IN THE PHARMACEUTICAL AND BIOTECHNOLOGY SECTORS BY THE REGIONAL OFFICES OF THE DGFT AS PER CUSTOMS NOTIFICATION NO 12/2012 DATED 17.03.2012 (erstwhile Notification No. 21/2002 Dated 01.03.2002)</title>
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    <description>Appendix 8A prescribes the application and certification process for export linked duty free imports by pharmaceutical and biotechnology units: applicant details, IEC, computation of entitlement from prior year physical exports, disclosure of cumulative imports and proposed CIF imports, and applicant declaration that imports are for manufacture, will not exceed the prescribed export linked proportion, will be installed within six months and not transferred for seven years, and that the unit&#039;s R&amp;D wing is registered with the Department of Science and Industrial Research. It requires a Chartered/Cost Accountant certificate and Regional Office verification to authorize duty free import subject to the Customs notification and penalties under the FTDR Act for misstatement.</description>
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    <pubDate>Wed, 15 Apr 2015 12:19:21 +0530</pubDate>
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      <link>https://www.taxtmi.com/acts?id=19540</link>
      <description>Appendix 8A prescribes the application and certification process for export linked duty free imports by pharmaceutical and biotechnology units: applicant details, IEC, computation of entitlement from prior year physical exports, disclosure of cumulative imports and proposed CIF imports, and applicant declaration that imports are for manufacture, will not exceed the prescribed export linked proportion, will be installed within six months and not transferred for seven years, and that the unit&#039;s R&amp;D wing is registered with the Department of Science and Industrial Research. It requires a Chartered/Cost Accountant certificate and Regional Office verification to authorize duty free import subject to the Customs notification and penalties under the FTDR Act for misstatement.</description>
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