Pharma Export  the Process Explained and the Value it Adds to the Market
                     Pharma Export: the Process Explained and the 
Value it Adds to the Market
How Can India Export Medical technologies?
•The IEC (Shipping Code) Number is the first important criterion. This number is provided for all import and export 
pharmaceutical products. You must apply to the Director General of Foreign Trade where your business is based.
•Without an IEC code, no items may be transported into or out of a country. Only licensed pharmaceutical companies are 
allowed to pharma export medicines from India by our foreign trade policy, thus the corporation must apply for an Import 
Export Permit and enroll with the Director-General of Foreign Trade.
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•Regulatory Conformity Businesses must examine the laws of the nation they are exporting from and formally register their 
goods there to prevent problems later. They must acquire the same clearance from India’s drug controller general after 
receiving it from the country that is importing the goods.
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•Market Investigation and Pharma Export Planning Business owners must make contact with individuals in the import and 
export  pharmaceutical products from India after they have all the necessary documentation to find a vendor or buyer who 
is interested. Pharma Company owners should investigate their options and select an appropriate shipping plan.
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•Valid Documentation Here, the buyer will provide a proforma invoice with the confirmation mail that contains information 
about the product, how much packing is required, and the delivery address to the pharma export companies in India. The 
firm must next produce a proforma invoice to be filed by this purchase requisition or Letter of Credit, according to how they 
intend to fund the order.
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•Easy And Trustworthy Shipping Business owners must get into a contract with the shipment or freight transportation 
provider to ensure efficient order fulfillment. To minimize unnecessary delays and problems, exporters should only send their 
goods through recognized companies.
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Where Can you Get a Valid Pharma Export License for 
Medicine?
• You must first get permission from the Indian government to export medication from India. There are a few things 
you should keep in mind, but the license application procedure is rather simple.
• Here is a brief explanation of how to accomplish it. You must first get a license application form from the Indian 
Directorate General of Foreign Trade (DGFT).
• The form is available online at www.dgft.gov.in or by getting in touch with the DGFT directly. After you obtain the 
form, complete it and submit it along with the amount required by the form back to the DGFT. You must next 
provide evidence that your medications adhere to all of the safety requirements established by Indian authorities. 
• This evidence might take the form of paperwork from your producer or supplier and lab test results attesting to 
the safety of your medications for export. Lastly, if the Indian government needs to approve your medications 
specifically, you will need to submit the required papers.
• How Much Does a License to Pharma Export Cost?
• You should be aware of the expense of obtaining a license if you want to export medicines from India. Although 
getting a license might be an expensive and time-consuming procedure, it’s crucial to keep in mind that you have a 
constitutional entitlement to do so. 
• This is a short tutorial on how to export medicines from India lawfully. You must first decide if you are qualified to 
obtain a license. Your business must fulfill specific conditions, which include holding a legitimate license to 
manufacture and distribute medicines in your nation of origin.
•  If you can demonstrate that the goods you’re exporting aren’t subject to any limitations, you could still be eligible 
to apply for a license even if your firm doesn’t currently have one. The very next step is to fill out an application 
once you have established that you are qualified for a license.
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Documentation Needed for India’s Pharma Exports
• Many statutory and regulatory regulations control the export of prescriptions from India. For instance, the 
Export Control Act of 1975 (ECA) regulates the export of technology and restricted items.
• Drug exports are governed by the Food and Drug Administration of India (FDA). In addition, the export of 
pharmaceutical items is governed by several bilateral trade agreements involving India and other nations.
• Restrictions for Importing Indian Pharmaceutical Goods
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• Exports and imports are important for any nation’s economy and progress. It is not expensive to import 
pharmaceutical items into the global market from India, but there are regulatory restrictions that must be 
met. The following are the requirements that must be fulfilled by importers under the law.
• The importer often does not need a license, however foods that are considered nutraceuticals do.
• The business may speak with the FDA and ask for a license from the US Food And drug regulations, and the 
Drug, and Cosmetic Act.
• After obtaining a license, an individual is required to notify the FDA of the items they wish to import via a 
prior notice outlining the importation.
• It’s time to complete the two pieces of paperwork that will be required to discharge the goods at the port 
to complete the importation process. The consignment’s entry summary and the pertinent invoices used 
to determine its value are
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Ahmedabad, Gujarat 380009
• Phone: 079 2640 5517
• Email: [email protected]
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