Exporting pharmaceutical products from India involves navigating regulatory requirements, understanding international market demands, and ensuring compliance with quality standards. Key steps include obtaining necessary certifications, adhering to export regulations, and establishing reliable distribution channels.
Tecnova provides specialized support for pharmaceutical exporters, offering expertise in regulatory compliance, market entry strategies, and logistics management. With Tecnova’s assistance, businesses can streamline the export process, ensure adherence to global standards, and effectively tap into international markets, facilitating successful pharmaceutical exports from India.
The Indian pharmaceutical industry is perhaps one of the biggest sectors in the country, both in terms of value and volume, anticipated to escalate by 12% CAGR by FY2030. The pharmaceutical sector provides impetus to the country’s economy. Globally, the country has secured the third position regarding pharmaceutical production by volume and ranked thirteenth in terms of sheer value.
Furthermore, the country is a global manufacturing and research pivot, holding a share of 5.92% of pharmaceuticals and drugs. In 2021-22, India exported US$ 24.62 billion of pharma products. The robust growth trajectory has made pharmaceutical sectors in India offer lucrative business opportunities.
Business owners must adhere to the following parameters before exporting pharmaceutical products.
Business owners must seek approval from the supreme pharma regulatory authorities like USFDA, CDSCO, etc., to ensure the safety and security of the masses. The CDSCO (Central Drugs Standard Control Organization) regulates all the particularities of drug export, import, sales, and clinical research. The FDA also promotes public health awareness and develops rules that all medicines must be clinically tested before marketing, preventing the ingression of violated medical products.
Here are the steps to Export pharmaceuticals from India:
Step 1: The first and foremost thing that every manufacturer must do is register themselves with Director- General of Foreign Trade and collect the Import Export Code.
Step 2: On applying for IEC (Import Export Code), companies or business owners must communicate with the interested vendor of the importing countries.
Step 3: Now look through the terms and conditions, rules, and laws of importing country and other particulars, helping them register products in the importing country without facing any further complications.
Step 4: Register the product from DCGI (Drug Controller General of India) upon receiving approval.
Step 5: Research and decide on the shipping method and payment mode.
Step 6: Now business owner will have to wait to get approval for the purchase order. Alongside preparing a proforma invoice containing vital information like packing type, product rate, freight details, etc.
Step 7: Based on how the business owner plans to finance an order, draft a frame of a commercial invoice against the purchase order sent by the buyer.
Step 8: Proceed to sign a contract with a freight forwarding agency to export the pharma product to the respective importing country.
Step 9: In this stage, business owners must complete the entire documentation process and head to custom clearance.
Step 10: Pharmaceutical products will be shipped to the designated importing country after receiving customs clearance.
It is imperative to note that customs clearance is also required in importing countries.
It is mandatory for an exporter to apply for an IEC number to initiate the process of exporting pharma products from India. Here are the steps that will guide business owners or any forms to do so:
Step 1: First, visit the official website of DGFT (Directorate General of Foreign Trade) and select the ‘Online application tab’.
Step 2: Now select ‘IEC’ from the drop-down menu and choose the ‘Online IEC application’ tab.
Step 3: To access the account, enter PAN and click on the Next button.
Step 4: Navigate to the ‘File’ tab and select ‘New IEC Application Details’.
Step 5: On selecting the tab, get redirected to the online form. Now fill it out with necessary information and attach relevant documents.
Step 6: Select the’ branch’ button if business owners would like to add inputs about their branches and head to the ‘Directors’ tab to provide information about the directors.
Step 7: Select ‘EFT’ to initiate an online payment, mention the amount details and pay the processing charge to complete the transaction and IEC application procedure.
Step 8: Applicants or business owners must get the hard copy and submit it to DGFT’s office.
There are several regulatory compliances that the Ministry of Health and Family welfare has laid out, which applicants must adhere to before exporting a pharma product from India. One of the daunting tasks in exporting medicinal products is to receive approval from the Drug Controller General of India. Hence, applicants must keep all necessary documents in order and abide by the laws.
It is absolutely important for exporters to factor in the following pointers before exporting pharmaceutical products from India:
Business professionals looking to export pharmaceutical products from India can take the comprehensive assistance of leading consulting firms in India like Tecnova. With their years of experience, these firms not only help global companies set up their businesses in the country but also provide prompt assistance to any Indian business owners to export their products outside the country’s periphery. The high-skilled professionals strive to ensure a fast and standard solution for individuals, along with helping them decipher the market strategies and comprehend the regulatory compliances set by importing countries.
These firms help Indian pharmaceutical conglomerates receive approval from India’s drug authority, helping clients spread their businesses outside the country and expedite sales. Hiring pharma regulatory consulting firms in India helps optimize the manufacturing process and addresses every sort of business challenge.
Such pharma regulatory consultants in India ensure the manufacturing of medicinal products happens in accordance with the set government rules and regulations. Furthermore, they help clients search for the right potential buyers, ensuring pharmaceutical companies achieve their goal of exporting their products.
India is the fulcrum of providing generic medicines to different parts of the globe. However, for exporting any medicine, a company is put through several legal implications. Only after receiving approval from higher authorities, one will qualify for shipping medicinal products to importing country. With due diligence and abiding by the legal compliances, a pharmaceutical company in India will be able to spread out its business footprint and gain access globally.
References
https://bit.ly/3OCbIx7
https://bit.ly/3S4garx
https://bit.ly/3z5ypEd
https://bit.ly/3vcuBQb
Exporting pharmaceutical products from India involves navigating regulatory requirements, understanding international market demands, and ensuring compliance with quality standards. Key steps include obtaining necessary certifications, adhering to export regulations, and establishing reliable distribution channels.
Tecnova provides specialized support for pharmaceutical exporters, offering expertise in regulatory compliance, market entry strategies, and logistics management. With Tecnova’s assistance, businesses can streamline the export process, ensure adherence to global standards, and effectively tap into international markets, facilitating successful pharmaceutical exports from India.
The Indian pharmaceutical industry is perhaps one of the biggest sectors in the country, both in terms of value and volume, anticipated to escalate by 12% CAGR by FY2030. The pharmaceutical sector provides impetus to the country’s economy. Globally, the country has secured the third position regarding pharmaceutical production by volume and ranked thirteenth in terms of sheer value.
Furthermore, the country is a global manufacturing and research pivot, holding a share of 5.92% of pharmaceuticals and drugs. In 2021-22, India exported US$ 24.62 billion of pharma products. The robust growth trajectory has made pharmaceutical sectors in India offer lucrative business opportunities.
Business owners must adhere to the following parameters before exporting pharmaceutical products.
Business owners must seek approval from the supreme pharma regulatory authorities like USFDA, CDSCO, etc., to ensure the safety and security of the masses. The CDSCO (Central Drugs Standard Control Organization) regulates all the particularities of drug export, import, sales, and clinical research. The FDA also promotes public health awareness and develops rules that all medicines must be clinically tested before marketing, preventing the ingression of violated medical products.
Here are the steps to Export pharmaceuticals from India:
Step 1: The first and foremost thing that every manufacturer must do is register themselves with Director- General of Foreign Trade and collect the Import Export Code.
Step 2: On applying for IEC (Import Export Code), companies or business owners must communicate with the interested vendor of the importing countries.
Step 3: Now look through the terms and conditions, rules, and laws of importing country and other particulars, helping them register products in the importing country without facing any further complications.
Step 4: Register the product from DCGI (Drug Controller General of India) upon receiving approval.
Step 5: Research and decide on the shipping method and payment mode.
Step 6: Now business owner will have to wait to get approval for the purchase order. Alongside preparing a proforma invoice containing vital information like packing type, product rate, freight details, etc.
Step 7: Based on how the business owner plans to finance an order, draft a frame of a commercial invoice against the purchase order sent by the buyer.
Step 8: Proceed to sign a contract with a freight forwarding agency to export the pharma product to the respective importing country.
Step 9: In this stage, business owners must complete the entire documentation process and head to custom clearance.
Step 10: Pharmaceutical products will be shipped to the designated importing country after receiving customs clearance.
It is imperative to note that customs clearance is also required in importing countries.
It is mandatory for an exporter to apply for an IEC number to initiate the process of exporting pharma products from India. Here are the steps that will guide business owners or any forms to do so:
Step 1: First, visit the official website of DGFT (Directorate General of Foreign Trade) and select the ‘Online application tab’.
Step 2: Now select ‘IEC’ from the drop-down menu and choose the ‘Online IEC application’ tab.
Step 3: To access the account, enter PAN and click on the Next button.
Step 4: Navigate to the ‘File’ tab and select ‘New IEC Application Details’.
Step 5: On selecting the tab, get redirected to the online form. Now fill it out with necessary information and attach relevant documents.
Step 6: Select the’ branch’ button if business owners would like to add inputs about their branches and head to the ‘Directors’ tab to provide information about the directors.
Step 7: Select ‘EFT’ to initiate an online payment, mention the amount details and pay the processing charge to complete the transaction and IEC application procedure.
Step 8: Applicants or business owners must get the hard copy and submit it to DGFT’s office.
There are several regulatory compliances that the Ministry of Health and Family welfare has laid out, which applicants must adhere to before exporting a pharma product from India. One of the daunting tasks in exporting medicinal products is to receive approval from the Drug Controller General of India. Hence, applicants must keep all necessary documents in order and abide by the laws.
It is absolutely important for exporters to factor in the following pointers before exporting pharmaceutical products from India:
Business professionals looking to export pharmaceutical products from India can take the comprehensive assistance of leading consulting firms in India like Tecnova. With their years of experience, these firms not only help global companies set up their businesses in the country but also provide prompt assistance to any Indian business owners to export their products outside the country’s periphery. The high-skilled professionals strive to ensure a fast and standard solution for individuals, along with helping them decipher the market strategies and comprehend the regulatory compliances set by importing countries.
These firms help Indian pharmaceutical conglomerates receive approval from India’s drug authority, helping clients spread their businesses outside the country and expedite sales. Hiring pharma regulatory consulting firms in India helps optimize the manufacturing process and addresses every sort of business challenge.
Such pharma regulatory consultants in India ensure the manufacturing of medicinal products happens in accordance with the set government rules and regulations. Furthermore, they help clients search for the right potential buyers, ensuring pharmaceutical companies achieve their goal of exporting their products.
India is the fulcrum of providing generic medicines to different parts of the globe. However, for exporting any medicine, a company is put through several legal implications. Only after receiving approval from higher authorities, one will qualify for shipping medicinal products to importing country. With due diligence and abiding by the legal compliances, a pharmaceutical company in India will be able to spread out its business footprint and gain access globally.
References
https://bit.ly/3OCbIx7
https://bit.ly/3S4garx
https://bit.ly/3z5ypEd
https://bit.ly/3vcuBQb