top of page
Search
Biopharmaceutical Alliance Launched by India, South Korea, US, Japan, and EU
The global biopharmaceutical sector has taken a significant step towards ensuring a resilient drug supply chain with the formation of the...
Jun 7, 20243 min read
Medical Device Regulations India - Frequently Asked Questions (FAQs)
Frequently asked questions (FAQs) regarding medical device registration and regulations in India
Jan 17, 20245 min read
Case Study: Streamlined India Registration and Market Entry for Europe Gel-Based Nail Polish Brand
Client: A prominent Europe-based Gel-Based Nail Polish brand with aggressive global market expansion plans. Problem Statement: The client...
Jan 11, 20242 min read
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...
Nov 9, 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
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
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
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)
Jun 19, 20232 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
CDSCO Pharmaceutical Regulations in India
Pharmaceutical regulations and registration are governed by Central Drugs Standard Control Organization (CDSCO) India
Jan 26, 202210 min read
Case Study: Global Regulatory Intelligence for Dental Brand
Analysis of regulatory pathway for registration of cosmetic/dental care products in target countries
Jan 17, 20222 min read
Insights
Global, Concurrent, Experience Based
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.
bottom of page