EASTLING BIOTECH
Anti-Aging
Herbal Extracts
Brain Health
Natural Sweetener
Cosmetic Raw Material
Nutrition Supplements
Customized peptides
Weight Loss
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About Us
Well-being Start with Eastling
Xi'an Eastling biotech Co., Ltd. is dedicated to the research and development, production, and sales of natural plant extracts; With nearly 15 years of experience in identifying, researching, developing, and producing active ingredients for medicinal plants, we focus on providing innovative products and services to customers in industries such as pharmaceuticals, health food, and cosmetics.
Eastling Biotechnology has established a global direct harvesting system for plant raw materials, ensuring the high quality and authenticity of raw materials, while also protecting the continuity and diversity of plants; Having strong research and development capabilities, we can develop more effective and specialized plant active ingredients for the pharmaceutical, health food, and cosmetics industries; We have established an advanced quality control system, and the quality control of our products depends on advanced testing instruments and high-level technical experts. The effective combination of the two forms Eastling's ability to quickly and rigorously control product quality.
We believe that natural active ingredients are the foundation of our service to customers. Scientific and effective production technology is the foundation for us to provide customers with specialized products. We have the ability to serve customers in the pharmaceutical, health food, and cosmetics industries, provide new product solutions, and add new value to their products.
Why Choose Us
Your Strategic CDMO Partner for U.S. & EU Regulated Markets
Commercial Excellence from Day One
We design for commercial success. Our process development focuses on scalable, robust, and cost-effective manufacturing that meets the stringent quality and regulatory expectations of the FDA and EMA, turning your candidate into a viable product.
Regulatory Strategy Built for Approval
Navigate complex pathways with confidence. Our seasoned regulatory experts, with direct agency experience, develop and execute submission strategies (IND/IMPD to NDA/MAA) that anticipate and address FDA/EMA requirements, accelerating your path to approval.
Seamless, Integrated Program Leadership
We don’t just manufacture; we own the journey. With dedicated program managers, we ensure flawless tech transfer, scale-up, and lifecycle management, providing a single point of accountability from development to commercial supply.
Proactive Regulatory Engagement
We position you for success in every interaction. We prepare comprehensive briefing packages, manage pre-submission meetings (Pre-IND, Scientific Advice), and lead clear, strategic communication with health authorities to align on requirements and de-risk your program.
Quality by Design & Proven Compliance
Trust is built on consistency. Our facilities and quality systems are designed and maintained to meet FDA 21 CFR Part 211 and EU GMP Annex 1 standards. Our validated processes and rigorous quality culture are proven through successful regulatory inspections.
End-to-End Market Access
Launch and sustain with a full-service partner. We provide comprehensive CMC support for global submissions and manage post-approval changes, variations, and lifecycle management, ensuring your product’s continuous compliance and supply in the U.S. and EU markets.
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