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CHECKLIST OF DOCUMENTS TO BE SUBMITTED FOR ISSUE OF MANUFACTURING LICENCE FOR MANUFACTURE OF UNAPPROVED/ APPROVED NEW DRUGS/ BANNED DRUGS ACTIVE PHARMACEUTICAL INGREDIENTS (APIs) SOLELY FOR EXPORT
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Log in to the electronic certificate of pharmaceutical system using your credentials.
02
Select the option to create a new certificate.
03
Fill out the required fields such as product information, batch number, expiration date, and manufacturing details.
04
Upload any necessary documents or attachments such as lab reports or quality control certificates.
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Review the information provided and make sure all fields are filled accurately.
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Submit the completed certificate for approval and validation.
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Once approved, the electronic certificate of pharmaceutical will be generated and can be downloaded or printed for use.

Who needs electronic certificates of pharmaceutical?

01
Pharmaceutical companies
02
Manufacturers of pharmaceutical products
03
Distributors of pharmaceutical products
04
Regulatory agencies overseeing pharmaceutical industry
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Electronic certificates of pharmaceutical are digitized certificates that provide information about the authenticity and quality of pharmaceutical products.
Pharmaceutical manufacturers, importers, and exporters are required to file electronic certificates of pharmaceutical.
Electronic certificates of pharmaceutical can be filled out online using the designated platform provided by the relevant authorities.
The purpose of electronic certificates of pharmaceutical is to ensure the traceability and authenticity of pharmaceutical products in the supply chain.
Information such as product name, batch number, manufacturing date, expiration date, and certificate of analysis must be reported on electronic certificates of pharmaceutical.
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