4th June, 2026 Drugs Controller General of India (DCGI), issued a formal circular directing all drug manufacturers and all stakeholders to ensure they have a working pharmacovigilance (PV) system in place — one that is fully compliant with the Drugs…
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- GMP Guidelines
Loan Licensing in Pharmaceutical Manufacturing: Key Principles, Guidelines, and Regulatory Framework
Loan licensing in pharmaceutical manufacturing plays a crucial role by allowing companies to outsource manufacturing or testing operations to third-party facilities. This setup, governed by the Drugs and Cosmetics Act, 1940, and the Drugs and Cosmetics Rules, 1945, helps pharmaceutical…
The Central Drugs Standard Control Organisation (CDSCO), under the Ministry of Health & Family Welfare, is India's principal regulatory authority for the registration and regulation of medical devices. The CDSCO ensures that medical devices available in the market are safe…
The quality of medical product should be maintained throughout their shelf life and storage play a crucial role in this process. Storage of medicinal product is not only just providing the physical space for keeping the material but it also…
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- GMP Guidelines
Glass containers used in pharmaceutical preparations are intended to come into direct contact with pharmaceutical preparations. Glass containers shall have a proper closure system. The containers are designed in a manner that the removal of contents is hassle free and…
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