Contract R&D & Custom Formulation for Manufacturers | Novoremedy

Pharmaceutical-Grade R&D for Manufacturers

Partner with The Center for Innovation & Science to develop superior products with advanced technologies and pharmaceutical expertise

✓ Custom Formulation Development
✓ Advanced Delivery Systems
✓ Formula Optimization
✓ Stability Testing & Analytics
✓ Tech Transfer Support
✓ Regulatory Consulting

Why Partner With Novoremedy R&D

The Center for Innovation & Science Advantage

🔬

Pharmaceutical Expertise

Our team brings decades of pharmaceutical R&D experience from major drug companies—applying drug development rigor to consumer products.

  • 505(b)(2) regulatory strategy
  • Advanced delivery system development
  • Pharmaceutical formulation science
  • ICH-guided stability programs
  • Quality by Design (QbD) approach
💊

Advanced Technologies

We bring pharmaceutical drug delivery technologies to supplements and cosmetics.

  • Sublingual delivery
  • Oral disintegrating tablets (ODT)
  • Osmotic controlled-release
  • Liposomal encapsulation
  • Nanoparticle formulations
  • Transdermal patches & microneedles

Proven Track Record

Successfully developed and launched products in both USA and Vietnam markets.

  • 12+ products developed and launched
  • 9 Vietnam MOH registrations (100% approval)
  • Hospital & pharmacy distribution
  • Pharmaceutical pipeline advancing

Our R&D Services

Comprehensive Development Services

Custom Formulation Development

Complete product development from concept to manufacturing-ready formula

Our Process:
1

Concept Development

  • Understand your vision and goals
  • Market research and competitive analysis
  • Scientific literature review
  • Ingredient selection (evidence-based)
  • Feasibility assessment
2

Prototype Formulation

  • Initial formula development
  • Multiple iterations and optimization
  • Sensory evaluation
  • Preliminary stability assessment
  • Dose optimization
3

Comprehensive Testing

  • Stability testing (ICH-guided)
  • Analytical method development
  • Dissolution testing
  • In-vitro bioavailability
  • Quality specifications
4

Scale-Up & Tech Transfer

  • Manufacturing process development
  • Scale-up trials
  • Technology transfer to your manufacturer
  • Batch record development
  • Manufacturing training
Timeline: 6-15 months (depending on complexity)
Investment: Contact for quote based on scope
Ideal For: Brands with unique product concepts, companies seeking innovation
Formula Optimization

Improve existing formulas for better efficacy, stability, or manufacturing

Why Optimize:
  • Enhance bioavailability (2-4x improvements possible)
  • Improve stability and extend shelf life
  • Better taste/texture for consumer acceptance
  • Reduce manufacturing issues
  • Cost optimization without compromising quality
  • Competitive differentiation
Examples:

Vitamin C Enhancement

Add liposomal delivery to vitamin C supplement

Result: 2-3x absorption improvement

Convenience Upgrade

Convert standard tablet to ODT format

Result: Faster action, no water needed

Probiotic Protection

Optimize for stomach acid survival

Result: Higher viable CFU delivery

Timeline: 3-8 months
Investment: Lower than full development
Ideal For: Existing products needing enhancement
Advanced Delivery System Integration

Apply pharmaceutical delivery technologies to your products

Sublingual Delivery

Rapid absorption, first-pass bypass, 15-30 min onset

ODT Technology

Convenience, fast disintegration, no water needed

Osmotic Release

Once-daily dosing, steady 12-24 hour release

Liposomal

Enhanced bioavailability, ingredient protection

Nanoparticles

Improved dissolution, enhanced absorption

Transdermal

Patches for cosmetics or supplements, sustained delivery

Benefits:
  • Significant competitive differentiation
  • Improved efficacy (clinical or perceived)
  • Premium pricing justification
  • Healthcare provider appeal
Stability Testing & Analytical Services

Comprehensive testing for product development or quality verification

Stability Testing

  • Accelerated (40°C/75% RH)
  • Long-term (25°C/60% RH)
  • Photostability studies
  • ICH-guided protocols

Analytical Testing

  • Identity verification (HPLC)
  • Potency/assay testing
  • Impurity analysis
  • Dissolution testing

Method Development

  • Custom analytical methods
  • ICH Q2 validation
  • Stability-indicating methods
  • Tech transfer to QC lab
Use Cases: Registration support, vendor verification, quality investigations, competitive analysis
Regulatory Support

Expert guidance on regulatory pathways and requirements

USA – FDA

  • DSHEA compliance review
  • NDI notifications
  • Claims substantiation
  • Label review (21 CFR 101)
  • GRAS status assessment

Vietnam – MOH

  • Dossier preparation
  • Local testing coordination
  • Submission & follow-up
  • 100% approval track record

505(b)(2) Strategy

  • IND preparation
  • CMC documentation
  • FDA communication
  • Approval pathway guidance

R&D Investment

Transparent pricing based on project scope

Formula Optimization $15,000 – $50,000
Custom Supplement/Cosmetic Development $50,000 – $150,000
Advanced Delivery System Integration $75,000 – $250,000
Pharmaceutical Development (505(b)(2)) $250,000 – $2,000,000+
Stability Testing (Standalone) $5,000 – $25,000
Vietnam Registration Service $35,000 – $75,000
Payment Terms: Milestone-based (50% deposit, remaining at milestones)
Note: Every project is unique. Request consultation for detailed proposal specific to your needs.

R&D Partnership Success Stories

Advanced Joint Supplement Development

Client:

USA supplement brand

Challenge:

Client wanted to develop premium joint supplement differentiating from crowded market with pharmaceutical-quality and natural ingredients.

Our Approach:
  • Literature review identified Boswellia as potent natural anti-inflammatory
  • Formulated with clinical doses (1500mg glucosamine, 200mg Boswellia)
  • Optimized delivery for enhanced bioavailability
  • Comprehensive 24-month stability testing
  • Tech transfer to client’s contract manufacturer
Results:
✓ Product launched successfully in USA
✓ Strong differentiation with Boswellia
✓ Positive market response
✓ Client expanded to full product line

Timeline: 10 months concept to manufacturing

Liposomal Vitamin C Optimization

Client:

Cosmetic brand (existing Vitamin C serum underperforming)

Challenge:

Client’s vitamin C serum had stability issues (oxidation, browning) and questionable efficacy. Wanted pharmaceutical-grade upgrade.

Our Approach:
  • Analyzed existing formula (identified instability causes)
  • Developed true liposomal vitamin C formulation
  • Verified liposome formation (particle size analysis, electron microscopy)
  • Comprehensive stability testing (6 months accelerated, ongoing long-term)
  • Enhanced with additional antioxidants and peptides
Results:
✓ Stable formulation (no browning 18+ months)
✓ Verified 3x enhanced absorption
✓ Superior customer feedback
✓ Premium pricing justified

Timeline: 7 months

Why Clients Choose Us

1. Pharmaceutical Pedigree

Team with decades of pharmaceutical R&D experience from major companies. We’re not supplement marketers—we’re pharmaceutical experts applying our knowledge to consumer products.

2. State-of-the-Art Facility

5,000 sq ft pharmaceutical R&D laboratory with HPLC, LC-MS, dissolution testing, stability chambers—equipment you won’t find at typical supplement companies.

3. Advanced Technologies

We offer pharmaceutical delivery systems rarely seen in supplements and cosmetics—creating true differentiation.

4. Comprehensive Services

From concept through commercial launch—we handle all aspects of development, not just formulation.

5. Regulatory Expertise

505(b)(2) pharmaceutical experience plus proven Vietnam registration success (9 products, 100% approval rate).

6. Proven Track Record

12+ products developed and launched, satisfied clients, real-world commercial success.

Let’s Discuss Your Project

Free consultation to explore how we can help

📞 Phone

USA: +1 404 820 4015

🏢 Location

Center for Innovation & Science
2001 Talmage Road
Ukiah, CA 95482

Three Simple Steps:

1. Request Consultation ☎️

Free 30-60 minute call to discuss your needs

2. Receive Proposal 📋

Detailed scope, timeline, and investment estimate

3. Begin Development 🚀

Agreement signed, project kicked off