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Medical Device Regulations in India : A Closer Look at CDSCO Application Forms
The Central Drugs Standard Control Organization (CDSCO) in India plays a pivotal role in regulating the manufacture, sale, and...
Oct 19, 20234 min read
Types of Medical Device Approval Licenses Issued by CDSCO in India
The healthcare sector holds a crucial position in safeguarding the nation's health, with an importance given to the safety, quality and...
Oct 5, 20236 min read
Demystifying the Role of Indian Authorized Agents in Medical Device Registration
In the intricate landscape of medical device regulations in India, the role of the Indian Authorized Agent (IAA) stands as a pivotal link...
Sep 11, 20233 min read
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...
Sep 1, 20237 min read
MedTech Incubators and Accelerators in India: A Guide for Innovator & Early Stage Entrepreneurs
Incubators and accelerators stand as two essential pillars for fostering creativity and accelerating business expansion for early stage entr
Aug 30, 20236 min read
Nutraceutical Regulation and Registration in India (FSSAI)
The Indian population's increasing trust in immunity-boosting supplements has significantly transformed buying behaviours and market...
Aug 30, 20234 min read
Asia - Contract Staffing & Hiring for Regulatory Affairs (Pharmaceuticals & Devices)
Artixio’s Contract Staffing solutions in Asia can be tailored to suit your needs and long term Regulatory Affairs strategy
Jul 31, 20232 min read
Government Schemes for Funding and Financing Medical Devices in India
India holds the 4Th largest medical devices industry in India with a huge capital. India has great skilled in the research and...
Jul 8, 20233 min read
Medical Devices Innovations in India
The medical device market in India is projected to grow at a CAGR of 15.7% between 2021 and 2026, reaching a size of USD 50 bn by 2030
Jul 8, 20233 min read
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
Jun 20, 20232 min read
Responsibilities of 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
Jun 20, 20233 min read
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)...
Apr 17, 20231 min read
Enabling Go/No-Go Decision for a Global Medical Devices Leader
Artixio’s team has decades of experience supporting strategic commercial decisions using primary market intelligence.
Jan 26, 20222 min read
CDSCO Pharmaceutical Regulations in India
Pharmaceutical regulations and registration are governed by Central Drugs Standard Control Organization (CDSCO) India
Jan 26, 202210 min read
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Deep dive and engage in insightful discourse driven by concurrent global regulatory scenarios, industry trends and Artixio’s real-time experience across the product value chain. Whitepapers, research articles, landscape reports and case studies to help you stay ahead of the curve.
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