top of page
Search
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...
Jun 11, 20244 min read
Managing CDSCO registration of Multiple Product Variations of Cosmetics in India
The cosmetic industry thrives on innovation and diversity, offering consumers a wide array of products to meet their varied preferences....
May 6, 20243 min read
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...
Mar 5, 20245 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
Pharma Regulatory Contract Staffing – A Solution for Marketed Products Management
Artixio offers pharma regulatory contract staffing solutions to address these key challenges in Asian countries
Jan 11, 20243 min read
Case Study: Successful Registration of Software as Medical Device (SaMD)assisting Surgical procedure
Client: The client, a pioneering European company specializing in advanced medical technologies, sought regulatory approval for its...
Jan 9, 20242 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...
Dec 2, 20233 min read
CDSCO Medical Devices Regulations In India
Medical devices are emerging globally and India serves as the 4th largest market in Asia for medical devices. India aims to accelerate...
Nov 25, 20238 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
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
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
Marketed Pharmaceutical Products Lifecycle Management in Asia
Artixio’s Proven Experience in Managing Lifecycle for Marketed Products in Asia
Jan 21, 20232 min read
Cosmetic Labeling Requirements - A Global Comparison
#cosmetic #labeling #usa #uae #mfds #southkorea #japan #singapore #india #australia #newzealand
Jan 31, 20221 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