Jun 73 min read

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...

Jan 175 min read

Medical Device Regulations India - Frequently Asked Questions (FAQs)

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

Jan 112 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...

Nov 9, 20236 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...

Sep 11, 20233 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 1, 20237 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...

Jul 8, 20232 min read

Government Schemes for Funding and Financing Medical Devices in India

In recent times, there has been a significant push from Government of India for funding and financing medical devices innovation and...

Jun 20, 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, 20231 min read

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

Jun 19, 20232 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)

Apr 17, 20231 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)...

Jan 26, 20227 min read

CDSCO Pharmaceutical Regulations in India

Pharmaceutical regulations and registration are governed by Central Drugs Standard Control Organization (CDSCO) India

Jan 17, 20222 min read

Case Study: Global Regulatory Intelligence for Dental Brand

Analysis of regulatory pathway for registration of cosmetic/dental care products in target countries

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.

global regulatory intelligence pharma medical device cosmetics food animal tool

Insights

Global, Concurrent, Experience Based

Get in touch

Our experts will be delighted to assist you with your global business needs.