Understanding the Significance of Design History File (DHF) in Medical Device Development
Health Canada Cosmetic Regulations in Canada
Understanding Quality System Regulations (QSR) under 21 CFR Part 820
ISO 13485:2016 Certification for Medical Devices Quality Management System
QMS Certification through Medical Device Single Audit Program (MDSAP)
COFEPRIS Technovigilance of medical devices in Mexico
Taiwan Food and Drug Administration (TFDA) Drug Regulations in Taiwan
CDSCO Regulation of Cosmetics in India
Taiwan Food and Drug Administration (TFDA) Medical Device Regulation in Taiwan
Cosmetics Labeling for COFEPRIS compliance in Mexico
Artixio’s Regulatory Support for a Chinese Pharmaceutical Manufacturer in Mexico
Notice of Operation : Essential Pre-requisite for registration of products with COFEPRIS, Mexico
Medical Device Registration Pathways in Mexico : Standard and Expedited Review Routes
National Pharmaceutical Regulatory Agency (NPRA) Regulation of Health Supplements in Malaysia
DIGIPRIS: Mexico COFEPRIS Digital Platform for Product Registrations and Regulatory Submissions
US FDA Modernization of Cosmetics Regulation Act of 2022 (MoCRA)
Regulation of Medical Devices with Philippines Food and Drug Administration (PFDA), Philippines
Thailand FDA Regulations of Food manufactured or imported in Thailand
Health Sciences Authority (HSA) Medical Device Dealers Licenses in Singapore
The Mexico COFEPRIS Good Manufacturing Practices (GMP) Requirements for Cosmetics
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.
