CPHI China 2026: Meet Runxin at Booth E3B42 in Shanghai

Three weeks ago, our team returned from Vitafoods Europe in Barcelona with notebooks full of conversations, trend observations, and new partnerships forming. Now we are packing again — this time for Shanghai.

From June 16 to 18, Shandong Runxin Biotechnology will exhibit at CPHI & PMEC China 2026 at the Shanghai New International Expo Centre (SNIEC). You will find us at Booth E3B42 in the Formulations and Excipients zone.

This is Asia's largest pharmaceutical trade show — 240,000 square meters of exhibition space, 3,600 exhibitors, and over 110,000 professionals from 150+ countries. If you are sourcing a contract manufacturing partner for dietary supplements, this is where the serious conversations happen.

What We Are Bringing to Booth E3B42

We are not coming to Shanghai just to hand out brochures. Here is what you can expect when you visit our booth.

Eight Dosage Forms, One Manufacturing Partner

Most contract manufacturers specialize in two or three formats. We produce across eight:

• Tablets — 2 billion units/year, including coated, chewable, effervescent, and bi-layer
• Hard capsules — 2 billion units/year
• Softgels — 1 billion units/year
• Gummies — 1 billion units/year
• Oral liquids — 100 million bottles/year
• Effervescent tablets — 500 million units/year
• Granules & solid drinks — 500 million units/year combined
• Soft capsules (liquid-filled) — 1 billion units/year

Why does this matter? Because the supplement market is shifting toward format-driven innovation. At Vitafoods Europe last month, we saw twist-off liquid capsules, fast-dissolving strips, and targeted-release tablets dominating the New Products Zone. Brands that want to differentiate through delivery format need a manufacturer who has actually run those production lines — not just read about them.

If you are deciding between a gummy and an oral liquid for your next product, we can run both through our facility and give you real production data on cost, stability, and timeline. That conversation is a lot more useful than a catalog page.

6,000+ Formulations and a Willingness to Co-Develop

Our formulation library includes over 6,000 proven recipes across functional categories — weight management, cognitive health, women's health, beauty-from-within, immune support, sports nutrition, and more.

But we do not just hand you a formula from the shelf. Every brand has different target markets, regulatory requirements, and competitive positioning. Our R&D team works with you to adapt or develop formulations that fit your specific needs — whether that means adjusting mineral forms to prevent interaction conflicts in liquid supplements, or designing a multi-pathway weight management formula that stands apart from generic products.

Bring your concept to Booth E3B42. We will walk through what is possible, what is challenging, and what the real timeline looks like.

Certification Portfolio That Opens Doors

We hold the certifications that global brands need to enter regulated markets:

• ISO 9001 / ISO 22000
• FSSC 22000
• GMP
• FDA registration
• HALAL
• SC license
• REACH registration (EU market)
• ECOCERT (organic formulations)

If you are entering the European market, we can walk you through our REACH-registered ingredient documentation. If you need HALAL-certified production, our facility is audited and approved. These are not just certificates on a wall — they are operational capabilities that affect every batch we produce.

Real Stability Data, Not Just Claims

One of the most talked-about issues at Vitafoods Europe was the gap between label claims and actual stability. Multiple industry professionals told us the same thing: many supplement brands have no idea whether their active ingredients are still present at the claimed levels after 12 months on the shelf.

We take a different approach. Our liquid supplement manufacturing process includes a four-stage scale-up model — from lab-scale (1-10L) through pilot (5-50L), scale-up (500-2000L), to full production (2000-10,000L+) — with stability checkpoints at every stage. We do not ship until we have data.

At our booth, ask us about our stability testing protocols. We will show you what real data looks like.

Trends We Are Tracking — And What They Mean for Your Product

Between Vitafoods Europe in May and CPHI China in June, we have had a front-row seat to how the global supplement market is evolving. Here are three trends we expect to dominate conversations at CPHI — and how they connect to what we do.

GLP-1 Companion Nutrition

Approximately 12% of US adults are now on GLP-1 medications. The supplement industry is scrambling to build companion products — high-protein shots for muscle preservation, micronutrient complexes for nutrient depletion, gut health support for GI side effects.

These products demand precision formulation and rigorous stability testing. A high-protein liquid shot that separates after three months on the shelf is worse than no product at all. Our experience with liquid supplement formulation — including pH management, preservative systems, and taste masking — positions us to help brands enter this category correctly from day one.

Women's Health With Real Science

The era of adding iron and folic acid to a label and calling it a "women's formula" is over. Brands are building multi-ingredient, multi-pathway formulations targeting menopause, prenatal nutrition, hormonal balance, and vaginal health — with clinically studied botanicals and targeted mineral complexes.

These formulations are technically demanding. Ingredient compatibility, bioavailability optimization, and regulatory compliance all require a manufacturer who understands the science behind the formula, not just the mechanics of production.

Longevity Beyond Anti-Aging

Longevity was one of the defining themes at Vitafoods Europe, and we expect the same energy at CPHI. But the conversation has shifted from "anti-aging skin products" to holistic healthspan — joint health, cognitive preservation, metabolic resilience, cardiovascular support.

For brands, this means formulations with more ingredients, more pathways, and more complexity. Launching these products successfully requires a manufacturer who can handle that complexity without cutting corners on stability, taste, or compliance.

Plan Your CPHI China 2026 Visit: Schedule a Meeting Early

CPHI China is enormous. Three days, 3,600 exhibitors, and 110,000 attendees. The most valuable conversations happen when both sides come prepared.

If you are planning to visit our booth, reach out before the show. Tell us:

• What product category are you developing?
• Which dosage format are you considering?
• What is your target market and timeline?
• Do you have an existing formula, or do you need formulation support?

We will prepare relevant samples, formulation case studies, and certification documentation specific to your needs. That way, when you walk up to Booth E3B42, we can skip the introductions and get straight to the conversation that moves your project forward.

The Details

After CPHI: Our Door Is Always Open

Not everyone can make it to Shanghai in June. If CPHI does not fit your schedule, our team is available year-round for virtual meetings, factory audits, and sample evaluations. Our facility in Qufu, Shandong is a 2-hour high-speed train ride from Shanghai — and we regularly host international visitors for on-site tours.

Whether you meet us at Booth E3B42 or connect with us online, the conversation starts the same way: tell us what you are building, and we will tell you how we can help.

Schedule a meeting at CPHI →

Shandong Runxin Biotechnology Co., Ltd. — 29 years of supplement manufacturing. 3,000+ brand partners. 6,000+ formulations. Eight dosage forms. ISO 9001/22000, FSSC 22000, GMP, FDA, HALAL, SC, REACH, ECOCERT certified.