Freyr offers regulatory intelligence services, focusing on global regulatory insights for various industries, including medicinal products, medical devices, cosmetics, food, nutraceuticals, biocides, and household chemicals. Their services include regulatory reports, newsletters, analytics, and consulting. They also provide digital tools such as Freyr IMPACT and Freya Intelligence for regulatory intelligence and global ingredients data. Additionally, Freyr offers webinars, whitepapers, case stud
joined at 4 months ago
The Role of AI in Regulatory Intelligence: An In-Depth Study
This blog talks about AI in Regulatory Intelligence, showing how it streamlines compliance, improves efficiency, and accelerates global market entry.
How Pharma Companies Use Regulatory Intelligence to Accelerate Global Submi...
This blog talks about how pharma companies use Regulatory Intelligence to accelerate global submissions with AI-driven monitoring, insights, and automation.
Top 10 Features to Look for in Regulatory Intelligence Tools
This blog talks about the top 10 Features of Regulatory Intelligence Tools, including global coverage, real-time alerts, analytics, and workflows.
Market Authorization & Cosmetic Registration in Japan
Learn steps & challenges in Japan’s cosmetic registration under PMD Act.
What Is Regulatory Intelligence? A Beginner’s Guide for Life Sciences
Regulatory Intelligence is the systematic process of collecting, analyzing & applying regulatory information, acts as a basic guide for LiveScience firms.
How to Set Up a Regulatory Intelligence Function in Your Organization
This blog talks about building a regulatory intelligence function in life sciences industries with strategies for FDA/EMA compliance and clinical trials.
Brazil Sanitizing Products: ANVISA Rules & Compliance Guide
A clear overview of ANVISA regulations for sanitizing products in Brazil.
Why eCTD v4.0 is Critical for Japan’s Regulatory Future
Japan’s Pharmaceuticals and Medical Devices Agency (PMDA) is set to make eCTD v4.0 submissions mandatory by 2026. This move follows a successful pilot in the se...
Labeling Requirements for Daily Chemicals in China
Learn about China’s mandatory labeling standards for household & personal care chemicals.
EU Deforestation Regulation (EUDR) & Supply Chains
Learn how the EU Deforestation Regulation (EUDR) affects global supply chains.
Japan PMDA eCTD v4.0 Submission Services & Solutions
Seamless PMDA-compliant dossier conversion, validation, and submission support – Empowering regulatory confidence, Connect with Japanese Regulatory Publishing E...
Top 6 Cosmetic Artwork Regulatory Risks
Learn how to identify & mitigate cosmetic artwork risks globally. Ensure claims, labeling, & packaging meet evolving regulations in every market. Learn...
AICIS Compliance: Chemical Regulations in Australia
Ensure full AICIS compliance in Australia. Learn how to register, categorize chemicals, & meet reporting rules. Expert support available from Freyr Solution...
510(k) vs. De Novo: Key Differences in FDA Approval Pathways for Medical De...
Medical device manufacturers entering the U.S. market must carefully evaluate the FDA regulatory pathways available to them. For most non–PMA (Premarket Approva...
Food Supplement Labeling Rules in the EU
Learn how to comply with EU supplement labeling laws and navigate harmonization rules. Ensure consistent packaging across all EU markets. Talk to our Experts no...
