Learn what OTC products are and how to start OTC product distribution in India. Understand drug licence, FSSAI, cosmetics, Ayurvedic products, pain gel, cough syrup, third-party manufacturing, advertising and retail marketing.
Learn how to start a Siddha pharmacy or medicine company, including Form 25-D manufacturing licence, Form 25-E loan licence, Schedule T GMP, third-party manufacturing and product approval.
Learn how to use Google Ads for pharma franchise and PCD lead generation, including keywords, Search campaigns, location targeting, negative keywords, landing pages, conversion tracking, qualified leads and healthcare advertising policies.
Learn seven practical ways to increase sales in pharmaceutical distribution. Understand fast-moving products, market gaps, product variety, add-on selling, inventory management, schemes, customer service, payment control and retailer relationships.
Learn how to register a pharmaceutical company in India, including OPC, LLP and Private Limited Company, SPICe+ procedure, DSC, DIN, PAN, GST, drug licence, trademark, documents, fees and pharma business requirements.
Learn how to start a veterinary medicine manufacturing unit in India, including Form 25/28 licences, Schedule M, veterinary vaccines, technical staff, labelling and withdrawal-period requirements.
Learn whether an Indian B.Pharm pharmacist can open a pharmacy in western countries. Understand UK GPhC route, OSPAP, USA FPGEC, Canada PEBC, Australia OPRA, pharmacist registration, pharmacy ownership and business requirements.
surgical cotton licence, cotton roll packing licence, Class A medical device registration, absorbent cotton repacking, MD-5 cotton manufacturing licence
Complete pharmaceutical manufacturing business plan covering revised Schedule M, plant layout, machinery, licences, manpower, project cost, working capital, capacity, break-even and GMP requirements in India.
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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