Who Is Responsible for Raw Material Procurement in Loan Licence Manufacturing?
Learn who is responsible for raw material procurement in loan licence manufacturing. Understand loan licence vs third-party manufacturing, raw material records, Dual Use NOC, principal manufacturer role, API conversion and agreement clauses.
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Can I Start a “Marketed By” Pharmaceutical Company Without Drug Licence?
Learn whether a marketed by pharmaceutical company can start without drug licence, including wholesale drug licence requirement, manufacturer–marketer agreement, direct supply, stockist role and marketer responsibility.
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Guidelines on How to Start an Ayurvedic Manufacturing Company in India
Learn how to start an Ayurvedic manufacturing unit in India, including Form 24-D and 25-D, Schedule T GMP, premises, technical staff, machinery, product approvals, quality control, investment and e-AUSHADHI licensing.
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What Does “Manufactured By ABC” and “Marketed By DEF” Mean in Pharma?
Learn what “Manufactured by ABC” and “Marketed by DEF” mean in pharma, how marketed by companies work, third-party manufacturing model, brand ownership, monopoly rights and competitor rate research.
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Difference Between Pharmaceutical Loan Licence, Third-Party Manufacturing and PCD/Franchise
Learn the difference between pharmaceutical loan licence, third-party manufacturing and PCD/franchise, including meaning, documents, investment, brand ownership, quality responsibility and best model for beginners.
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Use of “Marketed By” Address in Third-Party Pharma Manufacturing
Learn whether marketed by address should match wholesale drug licence address in third-party pharma manufacturing, and how pharma marketing companies should use office, GST and drug licence addresses.
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Is Drug Licence Required at the “Marketed By” Address for a Pharmaceutical Marketing Company?
Learn whether a pharma marketing company needs a drug licence at its Marketed by address, how marketer responsibility works, and best practices for wholesale licence, corporate office and labelled address.
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What Does a Third-Party Manufacturer Require: Only Active Ingredients or the Complete Formula?
Learn whether a third-party pharmaceutical manufacturer requires only active ingredients or the complete formula, who selects excipients, what information the marketer must provide, and when product development and regulatory approval are required.
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Why Do Third-Party Manufacturers Require a Trade Name or Brand Name Affidavit?
Learn why third-party pharma manufacturers require brand-name affidavits and Form 51, how to search and register pharmaceutical trademarks, and whether to protect the company name, product brands or both.
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Documents Required for Loan Licence Pharmaceutical Manufacturing in India
Learn the documents and procedure required for a pharmaceutical loan licence in India, including Forms 24-A, 25-A, 27-A and 28-A, host-manufacturer consent, GMP documents, product dossiers, API requirements and GST treatment.
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