Labelling plays a critical role in the regulatory oversight and safe use of medical devices. In India, medical device labelling is governed by the Central
July 11, 2025
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Labelling plays a critical role in the regulatory oversight and safe use of medical devices. In India, medical device labelling is governed by the Central
If you are a manufacturer or importer of cosmetics aiming to enter the Indian market, understanding and adhering to cosmetic label compliance regulations is essential.
The Drug Manufacturing License is a mandatory legal authorization required for any individual or company intending to manufacture drugs, medicines, or cosmetic products in India.
India’s cosmetics market is one of the fastest-growing sectors globally, driven by rising consumer demand for a wide variety of beauty and personal care products.
India’s medical device import landscape is governed by a structured regulatory framework under the Central Drugs Standard Control Organisation (CDSCO)—the country’s apex regulatory body for
India’s drug regulator, the Central Drugs Standard Control Organization (CDSCO), has issued major new guidelines for export No Objection Certificates (NOCs). Effective May 15, 2025,
The Central Drugs Standard Control Organisation (CDSCO) serves as India’s National Regulatory Authority responsible for overseeing pharmaceuticals and medical devices. Operating under the Directorate General
The Central Drugs Standard Control Organisation (CDSCO) has recently issued a pivotal guidance document aimed at ensuring the safe disposal of expired and unused medicines.
The Central Drugs Standard Control Organisation (CDSCO) is the national regulatory body responsible for overseeing the safety, efficacy, and quality of drugs, medical devices, and
We make compliance effortless and convenient. Our Team ensures that indian compliance are both easy and convenient for our clients. We strive to simplify the process, making it and hassle-free.