High-Stability Botanical Engineering:
Molecular Isolation & Contract Manufacturing
We solve the Stability Paradox of natural molecules through advanced HPLC-standardization and OEB-4 containment suites.
Verified Expert
"Verify HPLC Fingerprint consistency and USP <467> Solvent compliance before finalizing clinical formulations."
High-Potency Isolation
OEB-4 Containment suites for 99.5%+ bio-active monomers.
Standardized Extracts
HPLC-DAD Fingerprinting for multi-ton batch consistency.
Cosmetic Actives
EGT, Bakuchiol & TECA isolation for dermal repair systems.
Technical Dossier
Access full technical data: COA, MSDS, 1H-NMR & Stability Data.
Engineering Excellence: From Molecular Design to Industrial Supply
Our vertically integrated facility handles the most demanding formulation and regulatory requirements for global Life Science leaders.
Formulation R&D
Solving Active Fallout & Oxidation. We optimize pH ranges and antioxidant synergy to ensure molecular stability in complex delivery systems.
Molecular Isolation
Custom extraction protocols to achieve ≥99.5% Peak Purity. Specialized in isomeric separation and targeted marker enrichment.
Dosage Diversity
Integrated manufacturing for Capsules, Tablets, Liquid Tinctures, and Softgels. Customized particle engineering (Micronization).
Regulatory Support
Full Audit-Ready Documentation. We provide comprehensive DMF (Type II/IV), COA, MSDS, and Stability Data for global filings.
Custom Formulation
Struggling with ingredient degradation? Our R&D team provides antioxidant synergy analysis and pH stability optimization for complex delivery systems.
Particle Engineering
Utilizing Micronization (D90 < 10μm) to enhance the bioavailability of hydrophobic actives in your capsules and tablets.
Regulatory Compliance
Full technical dossiers (COA/MSDS/TDS) and DMF support provided to accelerate your FDA/EFSA market authorization.
The Engineering Moat:
Redefining the Industrial Standard
Compare how Exbiol’s pharmaceutical-grade protocols outperform generic manufacturing.
| Technical Parameter | Generic OEM Factory | Exbiol / Aiherba Standard |
|---|---|---|
| Detection & Identity How molecules are verified | Basic Marker Content (UV-Vis / Titration) |
HPLC-DAD Fingerprinting
Full phytochemical spectrum identity & Isomeric consistency verification. VALIDATED |
| Impurity Control Residual management | Standard Compliance (Basic Screening) |
HS-GC Molecular Screening
Residual solvent control strictly compliant with USP <467> Class 2/3. COMPLIANT |
| Stability Profile Shelf-life assurance | Estimated Projections (Accelerated Only) |
24-Month ICH Real-time Data
Stability studies under ICH Q1A(R2) guidelines for global market authorization. AUDIT_READY |
| Manufacturing Safety Risk mitigation | General GMP Workshop (Standard Hygiene) |
OEB-4 High-Containment
Isolated negative-pressure suites for High-Potency Active Ingredients (HPAI). ISO_CERTIFIED |
Precision Formulation Blueprints
Leveraging our 29-year isolation expertise, we offer pre-validated synergistic solutions designed for rapid market deployment. Each blueprint is optimized for stability and bioavailability.
High-Absorption
Longevity Blends
Engineered to solve the solubility paradox of Resveratrol using EGT as a synergistic antioxidant stabilizer. Targeted at cellular NAD+ and Mitophagy pathways.
Request Prototype Data →Clean-Label
Cognitive Shots
A fully water-soluble solution designed for RTD beverages. We utilize deodorized Lion's Mane isolates to ensure sensory integrity without bitter aftertaste.
Request Prototype Data →Post-Procedural
Skin Repair Actives
Optimized for skin barrier restoration. Our TECA isolation ensures zero phototoxicity, while Ectoine provides 24-hour hydration buffering.
Request Prototype Data →Technical Resource Center: Accelerating Global Launch Cycles
Access our validated engineering roadmaps and manufacturing dossiers. Designed to streamline R&D timelines and ensure regulatory readiness for market leaders.
From Molecule to Market:
The 30-Day Engineering Roadmap
A step-by-step guide for R&D heads to transition from lab-scale isolation to finished product authorization within 30 days. Covers stability locking and pilot-batch validation.
2026 Industrial OEM/ODM
Manufacturing Capability Catalog
Complete breakdown of our 26,000 sqm GMP facility, OEB-4 containment suites, micronization capacities, and current available technical dossiers (DMF/CEP).
OEM/ODM Formulation & Manufacturing FAQ
AiHerba operates under strict Non-Disclosure Agreement (NDA) frameworks. We can execute a mutual NDA within 24 hours. Your custom phytochemical blueprint is stored in an encrypted server with restricted access, ensuring that your unique formulation remains your exclusive competitive advantage.
By leveraging our AI-Precision Engineering database, we can predict ingredient interactions instantly. This shortens the prototype phase significantly. Custom pilot samples are typically dispatched within 2-4 Weeks, including initial Aqueous Stability and organoleptic testing.
We solve the "sedimentation" paradox using Liposomal CWD (Cold Water Dispersible) technology. Every custom formula undergoes ICH Q1A(R2) accelerated testing (40°C / 75% RH). We guarantee zero discoloration and >99% active retention for high-end Dermal Beauty Solutions.
As a leading botanical ingredients factory, we provide a complete Technical Package with every OEM order. This includes Shimadzu HPLC Fingerprints, USP <467> solvent residue reports, and cGMP facility certifications required for FDA, EFSA, or TGA registration.
We support brands at scale. Contract manufacturing MOQs are project-specific, generally starting from 100kg+ for powders or 10,000 units for liquid shots. We offer DDP (Delivered Duty Paid) terms via our North American hubs, handling all tax and duty clearance.