List of FSSAI-Permitted Products and Ingredients in Food and Dietary Supplements
Learn how FSSAI regulates health supplements and nutraceuticals, including permitted ingredient schedules, product approval, Relabeller licensing, third-party manufacturing and manufacturer verification in Delhi/NCR.
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How to Market the Products of a Particular Pharmaceutical Company
Learn how to market another pharma company’s products as a PCD franchisee or distributor, including drug licence, GST, monopoly agreement, company verification, product selection and ethical marketing.
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How to Start a Small-Scale Pharma Capsule Manufacturing Company in India
Learn how to start a hard-capsule manufacturing unit in India, including required space, machinery, HVAC, technical staff, Quality Control laboratory, Form 24 and Form 25 licensing, Schedule M and step-by-step setup.
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How to Start a Generic Medicine Marketing Company in India
Learn how to start a generic medicine company in India through third-party manufacturing, including entity selection, wholesale drug licence, GST, product selection, trademarks, NPPA pricing and distribution.
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Is It Mandatory to Register a Brand Name for OTC Products in India?
Learn whether trademark registration is compulsory for OTC products in India and what licences are required for Ayurvedic capsules, condoms, medicinal oils, cosmetics and pharma marketing businesses.
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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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Licence Required to Sell Natural Mineral Remedies in India
Learn whether a natural mineral that is crushed, screened and packed requires a drug, AYUSH, FSSAI or cosmetic licence, and how medicinal claims affect product classification.
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Is FSSAI Registration Mandatory for Veterinary Supplements?
Learn whether FSSAI registration is mandatory for veterinary feed supplements such as liquid calcium, how feed supplements differ from veterinary drugs, applicable licences, labelling and GST requirements.
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