The Center for Innovation & Science
Where decades of pharmaceutical expertise transform everyday health products
Pharmaceutical Rigor for Consumer Benefit
The Industry Challenge
The supplement and cosmetics industries often settle for ‘good enough.’ Standard formulations. Basic delivery methods. Minimal testing beyond regulatory requirements.
But consumers and healthcare providers deserve pharmaceutical-grade quality—not just in prescription drugs, but in the products they use every day.
- 📊 75% of supplements fail independent quality testing
- 🔬 Most cosmetics use delivery technologies from the 1980s
- 📉 Bioavailability often <20% with standard formulations
The CIS Approach
At The Center for Innovation & Science (CIS), we apply the same rigorous development processes used for FDA-approved pharmaceuticals to create superior supplements and cosmetics.
Our pharmaceutical-grade approach includes:
- Advanced formulation development
- Comprehensive stability testing (ICH-guided)
- Dissolution and bioavailability studies
- Analytical method development & validation
- Quality by Design (QbD) principles
- Scale-up and tech transfer expertise
The result? Products that work better, deliver more effectively, and meet the highest quality standards.
From Concept to Commercialization
Advanced capabilities across pharmaceutical, supplement, and cosmetic development
Developing Next-Generation Therapies
JAK3/TEC Inhibitor Topical Semisolid
Severe Spot Baldness (Alopecia Areata)Innovation: Targeted JAK3 and TEC inhibition through advanced topical delivery
- ✓ Targeted immunomodulation
- ✓ Topical delivery (reduced systemic exposure)
- ✓ Novel mechanism of action
- ✓ Potential for significant efficacy improvement
CGRP Receptor Antagonist Transdermal Patch
Migraine Headache TreatmentInnovation: Continuous transdermal delivery of CGRP receptor antagonist for sustained migraine prevention
- ✓ Non-oral delivery (avoids GI side effects)
- ✓ Sustained release (consistent blood levels)
- ✓ Improved patient compliance
- ✓ Convenient weekly application
Peptide Microneedle System
Advanced Delivery TechnologyInnovation: Microneedle technology for painless, self-administered peptide delivery
- ✓ Minimally invasive (painless)
- ✓ Self-administered (no healthcare visit needed)
- ✓ Controlled, sustained peptide release
- ✓ Improved bioavailability vs. oral delivery
Pharmaceutical Technologies for Daily Wellness
We’re revolutionizing the supplement industry by applying advanced pharmaceutical delivery systems to enhance bioavailability and efficacy. The result: supplements that truly work.
Sublingual Delivery
Active ingredients placed under the tongue absorb directly into the bloodstream, bypassing liver metabolism.
- ✓ Rapid onset (15-30 minutes)
- ✓ Higher bioavailability (60-70%)
- ✓ Lower dose required
- ✓ Reduced GI side effects
Oral Disintegrating Tablets
Tablets that disintegrate rapidly in the mouth (<30 seconds) without water.
- ✓ No water needed
- ✓ Fast disintegration and absorption
- ✓ Improved compliance
- ✓ Pleasant taste and mouthfeel
Liposomal Encapsulation
Actives encased in tiny lipid spheres that protect ingredients and enhance cellular delivery.
- ✓ Protection from digestive degradation
- ✓ Enhanced absorption (2-4x standard)
- ✓ Targeted cellular delivery
- ✓ Improved tolerability
Advanced Skincare Through Pharmaceutical Science
We bring pharmaceutical delivery technologies to cosmetics, creating products that don’t just sit on the skin—they penetrate effectively, deliver actives precisely, and produce visible results.
Liposomal Delivery
Phospholipid vesicles encapsulate actives and fuse with skin cells, delivering ingredients deep into the epidermis and dermis.
- ✓ Enhanced penetration (up to 12x)
- ✓ Sustained release of actives
- ✓ Protection of sensitive ingredients
Nanoparticle Formulations
Ultra-small particles (<100nm) that penetrate skin barriers and provide unique aesthetic benefits.
- ✓ Deep penetration
- ✓ Elegant, non-greasy feel
- ✓ Enhanced stability of actives
Microneedle Delivery Systems
Microscopic needles (<1mm) that painlessly penetrate the skin's outer layer and dissolve, delivering actives directly to target depths.
- ✓ Minimally invasive (painless)
- ✓ Direct delivery to dermis
- ✓ Enhanced efficacy of peptides
Pharmaceutical Experts, Consumer Product Focus
Led by Dr. Hiep X. Nguyen, PharmD, Ph.D., DTM, our team brings decades of pharmaceutical industry experience from major companies
505(b)(2) Regulatory Strategy
Decades of experience navigating the 505(b)(2) pathway
Novel Drug Delivery Systems
Expertise in transdermal patches, microneedles, controlled-release
Analytical Method Development
Development and validation per ICH guidelines
Formulation Science
Advanced formulation from concept through commercialization
Stability Studies
Comprehensive stability testing programs
Quality by Design (QbD)
Pharmaceutical QbD approach for robust development
Scale-up & Tech Transfer
Successful scale-up to commercial manufacturing
Clinical Trial Design
Experience with clinical protocols for pharmaceuticals
Your Questions Answered
Our team brings decades of pharmaceutical industry experience typically reserved for prescription drug development—505(b)(2) expertise, advanced delivery systems, comprehensive testing protocols, and regulatory knowledge. We apply these same rigorous pharmaceutical standards to supplements and cosmetics, resulting in products that simply work better.
We specialize in three main categories:
- • Pharmaceuticals: 505(b)(2) products, topicals, transdermal patches, microneedle systems
- • Dietary Supplements: Advanced delivery systems (sublingual, ODT, osmotic, liposomal), novel ingredients
- • Cosmetics & Cosmeceuticals: Pharmaceutical-grade skincare, liposomal products, peptide formulations, clean beauty
Timeline depends on product complexity:
- • Simple supplement reformulation: 3-6 months
- • Advanced delivery system (new): 6-12 months
- • Cosmetic product: 6-10 months
- • Pharmaceutical development: 12-36 months
We’ll provide a detailed timeline during project planning.
505(b)(2) is an FDA regulatory pathway that allows pharmaceutical developers to rely on existing published data for certain aspects of their product, rather than conducting all new studies. This significantly reduces development time and cost while still ensuring safety and efficacy.
Benefits: Faster to market, lower development costs, leverage existing data, still provides patent opportunities.
Costs vary based on project complexity:
- • Simple formulation: $15,000 – $50,000
- • Advanced delivery system: $75,000 – $250,000
- • Pharmaceutical development: $250,000 – $2,000,000+
During initial consultation (free), we’ll provide detailed cost estimates specific to your project.
Start Your Innovation Journey
Schedule a consultation to discuss your project
Schedule a Consultation
Direct Contact Information
📍 Address
2001 Talmage Road
Ukiah, California 95482
United States
📞 Phone
+1 404 820 4015
Monday-Friday, 9:00 AM – 5:00 PM PST
innovation@novoremedy.com
⏰ Response Time
We typically respond to inquiries within 1-2 business days
🏆 Success Metrics
9 Products Successfully Registered in Vietnam
- ✓ 100% approval rate
- ✓ Faster than industry average
- ✓ Zero rejections