India’s healthcare and pharma sectors are among the fastest-growing globally, with a strong focus on the safety, quality, and efficacy of drugs and medical devices. CDSCO registration, governed by the Drugs & Cosmetics Act, 1940, plays a vital role in this. CDSCO (Central Drugs Standard Control Organization), under the Ministry of Health & Family Welfare, is the national regulatory authority for drugs and medical devices in India.
CDSCO registration is not a simple process, but yes, it would be simple if proper knowledge is gained in CDSCO documents and guidelines and one goes by a systematic process. We are an Indian manufacturer or foreign manufacturer with ambitions in the Indian market, the correct CDSCO license or CDSCO import license is the beginning to abide by the law and a lucrative business in the long run.
The Central Drugs Standard Control Organization (CDSCO) is India’s national regulatory authority responsible for the approval, oversight, and regulation of drugs, medical devices, and cosmetics. Established under the Directorate General of Health Services, CDSCO ensures that products introduced into the Indian market are safe, effective, and compliant with regulatory standards.
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