TCI - The Global Leader in CDMO Solutions for the Nutraceutical & Skincare Industries
TCI is a leading global CDMO+ partnering with world-class brands to develop and manufacture functional supplements, functional foods, and high-performance skincare, from advanced formulation through large-scale production.
Why Partner with TCI?
TCI empower global brands with science-driven product design, robust intellectual property safety, and world-class automated manufacturing.
Years of Excellence
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Global Patents & Trademarks
What are you looking for?
Global Solutions. One Trusted Partner.
FAQ
- Concept & R&D: TCI screens natural ingredients with metabolic potential, utilizing cellular and clinical studies to evaluate them for satiety support development directions.
- Formulation & Stability: We integrate proprietary sustained-release technology to help maintain ingredient stability, while optimizing taste and user experience.
- Go-to-Market: We provide end-to-end "Joint Creation" services—from regulatory consulting and product positioning to marketing material support—to help customers transform R&D advantages into market-ready products.
Study results are obtained under defined research conditions and are not equivalent to finished-product effects. The claims a product can use depend on the complete formulation and target-market regulations.
- Stability Technology: To address the sensitivity of the DNA fragment ingredient, TCI utilizes micro-emulsification and innovative encapsulation technologies to stabilize the molecular structure, helping maintain activity in liquid formats.
- Absorption Enhancement: By leveraging osmotic pressure regulation and barrier-penetration technologies, we address traditional absorption limitations and support bioavailability in formulation design.
The DNA fragment ingredient is an ingredient for food applications, not a drug or an injectable product. Stability and absorption performance vary by formulation and delivery format and must be confirmed through separately designed testing.
- Scientific Anchoring: The core of development lies in "research evidence." We provide strictly validated formulations to support a solid scientific foundation for carbohydrate metabolism product development.
- Regulatory Compliance: TCI maintains a comprehensive global regulatory database, assisting customers in meeting international certification standards (e.g., FDA/EFSA/TFDA) to shorten Time-to-Market.
- End-to-End Manufacturing: From conceptual design to large-scale production, our highly automated smart factories support quality and capacity, helping customers capture early-mover advantages in the carbohydrate metabolism category.
Formulation validation does not establish a health effect for any finished product. Whether a product meets FDA, EFSA or TFDA requirements is determined case by case by the competent authority of each market.
The "Joint Creation" Model: TCI go beyond manufacturing by applying our IBD (Integrated Bioscience Design) methodology. By integrating consumer insights with genomic medicine and big data mining, we ensure every formula is designed for market success from day one.
- Phase 1: Insight & Trend Analysis: We analyze global market trends to lock in high-value product concepts.
- Phase 2: R&D & Validation: We develop formulations with scientifically anchored efficacy, supported by robust clinical data.
- Phase 3: Production & Quality Control: Our highly automated smart factories and rigorous quality standards (TCI Quality) ensure consistent, large-scale output.
- Phase 4: Market Support: We provide professional clinical reports and efficacy metrics to assist you in communicating effectively with your end consumers.
The above describes a service model; clinical data and efficacy metrics relate to the studies conducted and do not guarantee outcomes for any product. Deliverables and timelines are confirmed per project.
A Contract Development and Manufacturing Organization (CDMO) acts as a strategic business partner, taking health brands from initial concept to cross-border retail. Unlike traditional OEMs, a true CDMO+ like TCI seamlessly integrates advanced biological research, custom intellectual property (IP) creation, clinical trial validation, and fully automated, compliance-certified production (ISO, GMP).
The ISO and GMP certifications referred to here are held at company or factory level, not for any specific product or market. Actual service scope and deliverables are confirmed per project.
TCI utilizes well-established manufacturing systems to create delivery formats designed to support bioavailability and consumer palatability:
- Functional Liquids: Wellness shots, collagen drinks, and products utilizing our proprietary doubleNUTRI™ liposomal technology.
- Rapid-Dissolving Powders: Stable powders engineered to safeguard probiotic viability and active botanical strength.
- Nutritional Jellies: Great-tasting format packed with stable, maximum-dose active ingredients, suited to modern oral beauty and ingestible wellness positioning.
- Specialty Solid Doses: Rapid-disintegrating tablets, micro-capsules, and advanced delivery systems for beauty and daily wellness positioning.
The delivery format descriptions above are development directions, not substantiated performance of any finished product. Achievable addition levels, stability and permitted claims must be confirmed through formulation trials and target-market regulations.