Main Object Clauses
- To carry on the business of manufacturing, formulating, processing, packaging and marketing of pharmaceutical products including generic medicines, branded formulations, nutraceuticals, ayurvedic and herbal products, and veterinary medicines.
- To undertake contract manufacturing, loan licensing, third-party manufacturing and private labelling of pharmaceutical products for domestic and international pharmaceutical companies.
- To carry on the business of importing, exporting, distributing, wholesaling and retailing of pharmaceutical products, active pharmaceutical ingredients, excipients, surgical items and medical devices.
- To engage in pharmaceutical research and development, clinical trial support, bioequivalence studies, regulatory affairs consultancy and dossier preparation for domestic and international drug approvals.
NIC Code: 21 — Manufacture of pharmaceuticals, medicinal chemical and botanical products
Related Licences & Registrations
- Drug Manufacturing Licence: The State FDA issues manufacturing licences — no production without one, and Schedule M (GMP) compliance is physically inspected.
- WHO-GMP / COPP: Needed for export markets; domestic GMP is the baseline every unit must meet.
- CDSCO Registration: Required for importing drugs, medical devices and new formulations, and for clinical trial permissions.
ROC Filing Notes
- Pharma manufacturing objects are accepted at incorporation without a drug licence — the licence is post-incorporation, so the ROC does not demand it at the SPICe+ stage.
- Keep ‘retail pharmacy’ or ‘drug distribution’ as separate objects if the company will also sell directly — manufacturing and trading are distinct licensed activities and should read as such.
