Medical Device, Diagnostics Regulations in Taiwan FDA - Frequently Asked Questions (FAQs)
Medical Device Regulations India - Frequently Asked Questions (FAQs)
Pharmaceutical Artwork Management - Challenges and Solutions
Pharmaceutical Packaging Graphic Design - Challenges and Remediation
Case Study: Streamlined India Registration and Market Entry for Europe Gel-Based Nail Polish Brand
Pharma Regulatory Contract Staffing – A Solution for Marketed Products Management
Case Study: Successful Registration of Software as Medical Device (SaMD)assisting Surgical procedure
US FDA Guidance on Registration and Listing of Cosmetic Products and Facilities under Modernization of Cosmetics Regulation Act (MoCRA)
US FDA’s final guidance on Digital Health Technologies for Clinical Investigations
Pharmaceutical Regulations and Registration in Malaysia
Pharmaceutical Regulations in Thailand
Pharmaceutical Registration Process in Mexico (COFEPRIS)
The role of Australian TGA Sponsor for Therapeutic Goods Administration (TGA), Australia
The Cosmetic Product Notification(CPN)to National Pharmaceutical Regulatory Agency (NPRA), Malaysia
Nutraceutical Registration and Regulations in the UK (MHRA): A Comprehensive Guide
Demystifying the Role of Indian Authorized Agents in Medical Device Registration
Registration of Biologics in Malaysia (NPRA)
Medical Device Regulations and Registration in Canada (Health Canada)
Regulation of Health Supplements in Singapore
Medical Device Regulations in India (CDSCO)
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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.
