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FSSAI Labeling Requirements for Infant Formula in India

Ensuring the safety and quality of infant formula is paramount for the health and development of infants. In India, the Food Safety and...

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Managing CDSCO registration of Multiple Product Variations of Cosmetics in India

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The Food Safety and Standards Authority of India (FSSAI) Food Regulations in India

India's diverse culinary landscape is renowned for its rich flavors and cultural significance. However, behind the scenes, stringent...

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Medical Device Regulations India - Frequently Asked Questions (FAQs)

Frequently asked questions (FAQs) regarding medical device registration and regulations in India

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Client: A prominent Europe-based Gel-Based Nail Polish brand with aggressive global market expansion plans. Problem Statement: The client...

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Client: The client, a pioneering European company specializing in advanced medical technologies, sought regulatory approval for its...

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In the intricate landscape of medical device regulations in India, the role of the Indian Authorized Agent (IAA) stands as a pivotal link...

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Medical Device Regulations in India (CDSCO)

India's healthcare sector is witnessing significant growth, with a burgeoning market for medical devices. The regulation of medical...

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CDSCO Regulation of Cosmetics in India

Cosmetics play a significant role in our daily lives, enhancing our beauty and self-esteem. In India, the cosmetics industry has...

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In the intricate landscape of medical device regulations in India, the role of the Indian Authorized Agent (IAA) stands as a pivotal link...

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Biologics and Biosimilars Regulation and Registration in India (CDSCO)

The size of the Indian biosimilars market, which was anticipated to be worth $349 million in 2022, is expected to increase to $2108...

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Nutraceutical Regulation and Registration in India (FSSAI)

The Indian population's increasing trust in immunity-boosting supplements has significantly transformed buying behaviors and market...

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Named Patient Program in India (CDSCO)

The Named Patient Program approval process is designed to provide patients with access to investigational drugs that are not yet approved

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What are the Responsibilities of an Indian Authorized Agent for Medical Devices Import?

An Indian Authorized Agent must fulfill critical responsibilities detailed in the Medical Device Rules (MDR), 2017 to be able to import

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Regulations for Registration of Medical Device in India (CDSCO)

Regulations for Registration of Medical Device in India is overseen by the Central Drugs Standard Control Organisation (CDSCO)

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Updated List of Approved Fixed-Dose Combinations (FDC) from CDSCO, India

After identifying "certain typographical" flaws in the original document, India's Central Drugs Standard Control Organisation (CDSCO)...

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Marketed Pharmaceutical Products Lifecycle Management in Asia

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Cosmetic Labeling Requirements - A Global Comparison

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