OUR PHILOSOPHY
Pharmaceutical Rigor for Consumer Benefit
- Problem: Industry settling for “good enough”
- Solution: Apply pharmaceutical-grade R&D to supplements/cosmetics
- Side-by-side process comparison showing 10 steps vs. 5 steps
PHARMACEUTICAL DEVELOPMENT
- Advanced Formulation Design
- 505(b)(2) regulatory strategy
- Novel delivery systems (transdermal patches, microneedles, topicals)
- Analytical Development
- Regulatory Support
Current Pipeline:
- JAK3/TEC Inhibitor Topical – Severe alopecia treatment
- CGRP Antagonist Transdermal Patch – Migraine therapy
- Peptide Microneedle System – Advanced delivery
SUPPLEMENT INNOVATION
Advanced Delivery Systems:
- Sublingual Delivery (60-70% bioavailability vs 20-40% oral)
- Oral Disintegrating Tablets (ODT) – <30 second dissolution
- Osmotic Controlled-Release – 12-24 hour steady release
- Liposomal Encapsulation – 2-4x absorption enhancement
Development Process: 6 phases, 9-15 months total
- Phase 1: Concept Development (2-4 weeks)
- Phase 2: Formulation Development (8-12 weeks)
- Phase 3: Testing & Validation (12-16 weeks)
- Phase 4: Scale-Up (4-8 weeks)
- Phase 5: Tech Transfer (4-6 weeks)
- Phase 6: Launch Preparation (8-24 weeks)
COSMETIC & COSMECEUTICAL INNOVATION
Advanced Technologies:
- Liposomal Delivery – 12x penetration enhancement
- Nanoparticle Formulations – <100nm particles
- Microemulgels – Hybrid gel/emulsion systems
- Transdermal Patches – 8-24 hour sustained release
- Microneedle Delivery Systems – <1mm painless needles
First Launches:
- Novo Anti-Aging Serum (liposomal peptides)
- Novo Anti-Aging Cream (microemulgel base)
WORK METHOD
RESEARCH COLLABORATIONS
1
California Northstate University – Elk Grove, CA
- Academic research
- Student programs
- Clinical perspectives
2
Le Huu Trac National Burn Hospital – Hanoi, Vietnam
- Clinical testing
- Wound care development
- Real-world evidence
3
Hanoi University of Pharmacy – Hanoi, Vietnam
- Pharmaceutical research
- Quality methodologies
- Herbal expertise
EQUIPMENT & CAPABILITIES
Formulation Suite:
- High-shear mixers
- Homogenizers
- pH/viscosity control
- Specialized liposome/nanoparticle equipment
Analytical Laboratory:
- HPLC systems
- UV-Vis Spectrophotometer
- Dissolution testing apparatus
- Particle size analyzer
Quality Control:
- Environmental stability chambers (40°C/75% RH, 25°C/60% RH, 5°C)
- Microbial testing
- Hardness/disintegration testers
SUCCESS STORIES
Case Study: Vietnam Registration
- Challenge: Register 9 products with MOH
- Approach: Meticulous documentation, proactive communication
- Results: 100% approval rate, zero rejections
PARTNER WITH CIS
- Custom Formulation – Complete development service
- Contract R&D – Project-based research
- Regulatory Consulting – 505(b)(2), Vietnam MOH, FDA
- Quality Testing – Stability studies, analytical testing