Procedure and Criteria for submission and approval of applications for export of Diagnostic Kits and their components/laboratory reagents


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This notice details the procedure and criteria for applying for export licenses for Diagnostic Kits, their components, and laboratory reagents. A remaining export quota is available, and eligible exporters can apply online via the DGFT's ECOM system between March 4th and March 9th, 2021. Applications will be examined based on specific criteria, including proof of manufacturing and fulfilment of domestic commitments.

Ministry of Commerce 86 Industry Directorate General of Foreign Trade Export Cell Date:2nd March, 2021 Trade Notice No. 45/2020-21 To 1. All Members of the Trade 2. All DGFT RAs 3. All Custom Authorities Subject: Procedure and Criteria for submission and approval of applications for export of Diagnostic Kits and their components/laboratory reagents. Reference is invited toDGFT Notification No. 09 dated 10.06.2020restricting the export of Diagnostic Kits/Laboratory Reage
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FAQ :

Applications for export licenses must be submitted online between March 4th and March 9th, 2021.

Exporters must file applications online through DGFT's ECOM system for Export authorizations. No hard copies are required.

The remaining quota includes RT-PCR Kits (COVID/Non-COVID) or their components, RNA Extraction Kits or their components, and VTM Kits or their components.

Applicants must provide documentary proof of manufacturing the specified kits and fulfil domestic commitments. Only one application per IEC will be considered during this period.

Required documents include a copy of the purchase order/invoice and an undertaking from the manufacturer certifying that all domestic commitments have been fulfilled. All documents must be self-attested.

The validity of the export license will be for 6 months only.

 

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