We are glad to announce that Freyr is exhibiting at the DIA CHINA 2025, to be held at the Shanghai Zhangjiang Science Hall, China from May 22^nd to 25^th, 2025.

Meet us at Booth #D21 to meet the most revolutionary and gain insightful information on global Regulatory trends and Innovative technologies. Our colleagues Sathya K, Suresh Modugu, Praveen Bezawada, Fengqin (Jane) Zhang, Mandy Zhao and Lisi Huang will be delighted to meet you in person.

Join us as we showcase Freya Fusion, our AI-powered Regulatory platform, along with our comprehensive end-to-end Regulatory services across key markets including the US, EU, China, and Japan. Discover how our flexible staffing solutions, trusted by global pharmaceutical leaders in over 120 countries, can support your Regulatory success.

Visit our booth to explore how Freyr can empower your Regulatory journey.

Sathya K

Senior Vice President, MPR Excellence Group

Suresh Modugu

Assistant Vice President, MPR Regulatory Affairs

Praveen Bezawada

Chief Technology Officer

Fengqin (Jane) Zhang

Senior Director, MPR Regulatory Affairs

Mandy Zhao

Associate Director,MPR Sales

Lisi Huang

Business Lead, Business Strategy & Growth

Aspect	USA	EU	Australia	China	UAE
Regulatory Authority	FDA	EFSA & Member State Authorities	FSANZ	SAMR & NHC	ESMA & MOHAP
Major Regulation Governing Compliance	Federal Food, Drug, and Cosmetic Act (FFDCA); 21 CFR Part 110 (Current Good Manufacturing Practices)	Regulation (EC) No 178/2002 (General Food Law); Regulation (EU) No 1169/2011 on Food Information to Consumers	Food Standards Code (Australia New Zealand Food Standards Code)	Food Safety Law of the People's Republic of China (Revised 2015); GB Standards for Food Safety	UAE.S GSO 9:2017 (GCC General Requirements for Prepackaged Food)
Pre-market Approval Required?	No pre-market approval except for novel ingredients, color additives, or specific claims	No pre-market approval for general foods, but novel foods or health claims require EFSA approval.	No pre-market approval unless it's a novel food or makes health claims	Pre-market registration is required for novel foods, health foods, or products with new ingredients	Pre-market approval is required for certain foods, health products, and products with new ingredients
Processed Food Labeling Compliance /Labeling Requirements	Mandatory labeling as per FDA guidelines (Nutrition Facts, Ingredient Declaration, Allergens)	Must comply with EU Food Information Regulation (1169/2011); includes allergens, nutrition, and origin labeling.	Must follow FSANZ Food Standards Code for labeling; nutrition panels, allergens, and ingredient lists required	Must follow GB 7718-2011 (National Food Safety Standards) for labeling; mandatory nutrition facts, allergens, and shelf-life	Must follow GSO 9:2017 for pre-packaged food labeling; Arabic labeling, allergens, and nutrition facts required
Timeline for Registration	No fixed timeline: products can enter the market once compliant	No formal registration unless novel food; EFSA approval for health claims takes 12-18 months	No formal registration unless it's a novel food or makes health claims	Typically, 12-24 months for novel foods, shorter for regular processed foods	Approval may take 6-12 months for certain products. Regular processed foods can enter the market once label approval is obtained

Medicinal Products Regulatory Services

Medical Devices Regulatory Services

Consumers

Freyr Digital

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DIA CHINA 2025