Market Access for Innovative Feed Ingredients in China, the US and the EU

Background

As the global feed and pet food markets continue to expand, innovative feed ingredients are creating new opportunities for ingredient manufacturers, animal nutrition companies and pet food producers. China, the United States and the European Union represent key markets, but their regulatory frameworks, market access pathways and technical requirements differ substantially. Evolving regulatory procedures and scientific guidance add further complexity, particularly for microbial and fermentation-derived products. Selecting an unsuitable pathway or overlooking critical data requirements can lead to additional studies, prolonged review and delayed market entry.

Early regulatory planning is therefore essential to bringing innovative feed ingredients to market. In this webinar, Jasmine Luan, Regulatory Affairs Specialist, will compare the regulatory frameworks, competent authorities and market access pathways in China, the US and the EU. She will examine core technical requirements, opportunities for data reuse and market-specific considerations. Illustrative product cases will show how pathway selection, study planning and data protection affect submission strategies, timelines and commercialization, helping companies prepare for market entry and avoid common regulatory pitfalls.

To have a better chance of your questions being addressed, you’re welcome to email us the questions before the webinar.

Contents

Part 1 — Introduction and Product Positioning

• 1.1 Standard Definitions and Scope of Innovative Feed Ingredients

• 1.2 Product Classification and Positioning for Market Entry

• 1.3 Assessment of Existing Regulatory Status

Part 2 — Market Access Pathways in China, the US and the EU

• 2.1 Regulatory Framework Comparison

• 2.2 Step-by-Step Approval Procedures and Access Routes

• 2.3 Pathway Comparison and Selection Criteria

Part 3 — Core Compliance Requirements and Data Optimization

• 3.1 Manufacturing Specifications and Product Identity Criteria

• 3.2 Safety and Efficacy Dossier Preparation Guidelines

• 3.3 Cross-Border Data Reuse Strategies to Reduce Testing Costs

Part 4 — Commercial Strategies, Timelines and Risk Management

• 4.1 Time and Cost Estimations

• 4.2 Data Protection and Commercial Rights

• 4.3 Submission Planning and Market Launch

The final outline may be subject to minor revisions.

Schedule

Speakers

Jasmine Luan - Regulatory Affairs Specialist

REACH24H

Jasmine Luan, graduated from Zhejiang University with a master's degree in Food Engineering, is now working as a regulatory affairs specialist in REACH24H. She possesses years of experience in food research and is well-versed in domestic and international food and feed regulations and standards. She can provide professional regulatory consulting, product compliance consulting, product registration, and other related services for enterprises.