Process & Methodology

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A systematic, science-backed approach to formulation development

At Formulyn, every formula I create follows a rigorous methodology honed through years of pharmaceutical and nutraceutical R&D. Here's exactly what you can expect when we work together:

What happens:
I start by understanding your vision, target market, and goals. We'll discuss desired benefits, target demographics, price points, and any specific requirements.

What you provide:

• Product concept and intended benefits
• Target audience details
• Budget and timeline parameters
• Any existing research or competitor products

What you receive:

• Initial feasibility assessment
• Preliminary ingredient recommendations
• Project timeline and milestones
• Transparent project quote

What happens:
I dive deep into scientific literature, reviewing clinical studies and efficacy data for relevant ingredients. I design your formula architecture, selecting ingredients based on synergy, bioavailability, and evidence.

My methodology:

• Evidence-based ingredient selection (peer-reviewed research)
• Dosage optimization for clinical efficacy
• Compatibility and stability analysis
• Regulatory compliance screening (TGA/FDA)
• Cost-efficiency evaluation

What you receive:

• Detailed formulation blueprint
• Ingredient rationale (why each ingredient, at what dose)
• Regulatory compliance overview
• Alternative options if applicable

What happens:
I finalize the formula specifications, calculate precise dosages, and develop complete manufacturing documentation. I assess stability, shelf life, and identify potential challenges.

Quality checks:

• Ingredient interaction screening
• Stability predictions and testing recommendations
• Organoleptic properties (taste, smell, texture)
• Packaging compatibility
• Manufacturing feasibility

What you receive:

• Final formulation specifications
• Complete ingredient list with CAS numbers
• Manufacturing instructions
• Quality control parameters
• Certificate of Analysis requirements

What happens:
I prepare comprehensive documentation that manufacturers need, along with guidance for your next steps.

What you receive:

• Master formula document
• Manufacturing SOPs (Standard Operating Procedures)
• Quality specifications
• Supplier recommendations
• Regulatory documentation support
• Label compliance guidance
• 30 days of post-project support for manufacturer questions

What happens:
As you move into manufacturing and launch, I'm available for technical support, troubleshooting, and optimization.

Available support:

• Manufacturing partner liaison
• Batch testing interpretation
• Formula adjustments based on production feedback
• Scaling recommendations
• Reformulation for cost or supply changes

Every formula I develop adheres to:

✓ Evidence-based formulation - Every ingredient backed by clinical research
✓ Regulatory compliance - TGA, FDA, and GMP standards built in from day one
✓ Manufacturing viability - Formulas designed for real-world production, not just theory
✓ Transparent documentation - Clear, comprehensive specs manufacturers can work with
✓ Ethical formulation - No pixie-dusting, no misleading claims, no cutting corners

I don't just create formulas - I create launchable products.

Many formulators hand you a list of ingredients and call it done. I provide everything you need from concept to manufacturing floor:

• Regulatory-ready documentation
• Manufacturing troubleshooting built in
• Cost-conscious without sacrificing efficacy
• Clear communication at every stage
• Real-world production experience, not just textbook knowledge

Y

ou're not just getting a formula. You're getting a strategic partner who wants your product to succeed.