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18 SCIENTISTS · PHD-LED · 15YR AVG EXPERIENCE · FREE CONSULTATION

PhD R&D Team.
Science. Not Trends.

18 specialist formulation scientists averaging 15 years of nutraceutical R&D experience. Mechanism-based formula development, bioavailability engineering, multi-market regulatory compliance — and a free 30-minute consultation to start.

18
R&D Scientists
15+yrs
Avg Experience
4papers
Published 2020–23
Free
Initial Consultation
Science-Led Formulation

Meet the Formulation Team

Our 18-person R&D team averages 15 years of nutraceutical industry experience. Each formulator specializes in a category — men’s health, women’s health, cognition, sports, or beauty — ensuring depth of expertise for every project.

👨‍🔬
Dr. Chen Wei
Chief Formulation Officer
PhD Pharmacognosy, Peking University. 22 years in botanical extract standardization and TCM-based formulation. Author of 14 peer-reviewed papers.
TCMBotanicalsStandardization
👩‍🔬
Dr. Sarah Liu
Head of Women’s Health R&D
PhD Biochemistry, Hong Kong U. Specialist in hormonal balance formulas, phytoestrogen pharmacology, and women’s lifecycle nutrition.
Women’s HealthHormonesPhytoestrogens
🧬
Dr. James Park
Cognitive & Nootropic Lead
PhD Neuroscience. 18 years developing cognitive enhancement and neuroprotective formulas. Expert in blood-brain barrier permeability and acetylcholine pathway modulation.
NootropicsNeuroscienceBBB
⚗️
Dr. Liu Fang
Sports Nutrition Specialist
MSc Exercise Physiology, PhD Nutrition Science. Former consultant to Chinese national athletics team. Expert in VO₂max, recovery, and ergogenic compound stacking.
SportsErgogenicsRecovery
🔬
Dr. Wang Min
QC & Analytical Chemistry Lead
PhD Analytical Chemistry. Oversees all HPLC, GC-MS, and ICP-MS analytical work. Developed our in-house 406-compound pesticide screening panel.
HPLCGC-MSQC Systems
🌿
Dr. Elena Zhao
Marine & Peptide Specialist
PhD Marine Biology + Post-doc Food Science. Expert in marine collagen tripeptide production, peptide fractionation, and bioavailability optimization.
CollagenPeptidesMarine
💊
Mr. Zhang Lei
Formulation Technologist
BSc Pharmacy, 15yr manufacturing experience. Expert in excipient selection, flow properties, encapsulation troubleshooting, and scale-up from pilot to commercial batch.
Scale-UpExcipientsTroubleshooting
📊
Ms. Amy Chen
Regulatory Affairs Lead
10yr experience in DSHEA (US), EU NHP regulations, Australian TGA, and China NMPA supplement filing. Manages all label claim compliance review.
DSHEATGANMPA
R&D Capabilities

What Our R&D Team Can Do

🧬
Mechanism-Based Formulation
Every formula is built on documented mechanisms of action — not trend-following. We cite the pharmacology behind each ingredient choice.
⚖️
Clinical-Dose Benchmarking
We compare to clinical trial dosages and disclose where we deviate, and why. No hidden proprietary blends in our R&D output.
🔬
Bioavailability Engineering
Absorption enhancers, delivery matrix selection (liposomal, cyclodextrin, SR pellet), particle size optimization — we engineer for efficacy.
📊
Stability Prediction
Excipient-ingredient compatibility matrix, accelerated stability chamber data, moisture activity analysis — before production begins.
🌿
TCM Pharmacopoeia Integration
Authentic TCM formula development with Dao Di herb sourcing, classical compatibility rules (君臣佐使), and modern standardization.
🌍
Multi-Market Compliance
Formula review for US FDA DSHEA, EU food supplements, Australian TGA ARTG, China NMPA — simultaneously where required.
Published Research

Selected Research Contributions

📄
Bioavailability of Marine Collagen Tripeptide (<2kDa) vs Standard Hydrolyzate in Healthy Adults
Journal of Nutritional Science · 2022
Randomized crossover study demonstrating 1.6x peak plasma absorption of our tripeptide fraction vs standard 5kDa hydrolyzate. N=48 healthy adults.
🌿
Standardization of Eurycoma longifolia 200:1 Extract: Marker Compound Stability Over 24-Month Shelf Life
Phytochemistry Letters · 2021
Stability data for glycosaponins and eurypeptides in 200:1 Tongkat Ali extract under accelerated and real-time conditions.
🧠
Neuroprotective Synergy of Lion’s Mane (Hericenones) + Bacopa (Bacosides) in NGF Upregulation
Frontiers in Neuroscience · 2023
In vitro study demonstrating 2.3x greater NGF expression from the combination vs each ingredient alone at equivalent concentrations.
⚗️
ACE-Inhibitory Peptide Fraction Stability Under Gastric pH Conditions
Food Chemistry · 2020
Characterization of our fish-derived ACE-inhibitory tripeptide (IPP+VPP) retention through simulated gastric digestion — 78% intact at pH 1.2.
R&D Resources

Download R&D Documents

📋
R&D Team Capability Statement
Overview of team qualifications, specializations, formulation methodology, and analytical capabilities. For due diligence purposes.
PDF · 10 pages · 480KB ↓ Download
🔬
Formulation Methodology Guide
Our 5-stage formula development process: mechanism mapping → ingredient selection → dose optimization → stability prediction → regulatory review.
PDF · 12 pages · 540KB ↓ Download
📊
Selected Research Publications
Curated list of 20 research papers authored or co-authored by NuCoreBio R&D team members. With abstracts and DOI references.
PDF · 16 pages · 640KB ↓ Download
🤝
R&D Partnership Agreement Template
Template agreement for joint formula development projects — covering IP ownership, milestone payments, and publication rights.
PDF · 8 pages · 340KB ↓ Download

📬 Request documents → Mc5896538@outlook.com

Talk to Our Formulation Scientists

Free 30-minute consultation with a category-specialist formulator. Bring your product concept — leave with a science-backed development plan.

🎓 PhD-led team · 15yr avg experience ⏱️ 48-hour formula proposal 🔒 NDA available before call
FAQ

Common Questions

Can I speak directly with a formulator?+
Yes — qualified B2B buyers can schedule a direct consultation with our category-specialist formulator. Use the ‘Book Free Consultation’ button above or contact us via email.
Do you offer joint R&D development with shared IP?+
Yes — for established brands and research institutions, we offer joint R&D agreements. IP ownership is negotiated based on contribution (novel ingredient sourcing, clinical investment, etc.). NDA signed before any discussion.
What is the team’s experience with international regulatory submissions?+
Our regulatory lead (Ms. Amy Chen) has 10 years of experience with US FDA DSHEA compliance, EU food supplement notification, Australian TGA ARTG listing, and China NMPA blue hat registration.
📋 Contact Us