Formulation, Compliance Review & CMO Transfer
I help brands build products that are formulation-ready, compliance-aware, and manufacturable before capital is committed.
How I Structure Projects
Phase 1 — Product Architecture Roadmap
Phase 3 — CMO Transfer & Manufacturing Readiness
Phase 1 — Product Architecture Roadmap
Define the product strategy before formulation begins.
- Product positioning and use-case logic
- Claim posture and regulatory exposure
- Ingredient direction, sourcing risks, and CMO pathway
Phase 2 — Formula & Compliance Lock
Phase 3 — CMO Transfer & Manufacturing Readiness
Phase 1 — Product Architecture Roadmap
Turn the roadmap into a formulation-ready product system.
- Formula development or refinement
- Supplement Facts, claims, and documentation structure
- Testing strategy, COA/spec review, and production readiness
Phase 3 — CMO Transfer & Manufacturing Readiness
Phase 3 — CMO Transfer & Manufacturing Readiness
Phase 3 — CMO Transfer & Manufacturing Readiness
Prepare the product for manufacturer review and production.
- Quote-ready formula and production documents
- Process notes, packaging assumptions, and testing expectations
- CMO handoff support to reduce manufacturing drift
About Me
Independent Supplement Product Development Consultant
My background combines 17+ years in pharmaceutical R&D and QA systems with an independent consulting track record of 400+ developed products across capsules, powders, liquids, gummies, pet products, functional beverages, topicals, and specialty nutrition formats.
Through Clean Label Supplements, I provide independent product-development consulting using a clean-label, manufacturing-first approach.
The goal is simple: build products that are clear, defensible, manufacturable, properly documented, and ready for real-world execution.
Built on Real Product Development Experience
Pharma R&D + QA Systems Foundation
Pharma R&D + QA Systems Foundation
Pharma R&D + QA Systems Foundation
17+ years in pharmaceutical R&D and quality systems, with hands-on experience in lab work, batch execution, process troubleshooting, SOPs, validation support, training, change control, and regulated documentation.
400+ Products Developed
Pharma R&D + QA Systems Foundation
Pharma R&D + QA Systems Foundation
Independent consulting track record across capsules, powders, gummies, liquids, pet products, functional beverages, topicals, and specialty formats.
Compliance-Aware Review
Compliance-Aware Review
Compliance-Aware Review
FDA / DSHEA-aware review of formula logic, claims, Supplement Facts structure, ingredient declarations, sourcing, COAs, and documentation gaps.
CMO Transfer Focus
Compliance-Aware Review
Compliance-Aware Review
Product documentation, process notes, testing expectations, packaging assumptions, and quote-ready handoff support for CMO review.
What Clients Say About Working With Me
Yoavb - Formulation & Strategy Consult
“Very impressed. This was a great decision to pick Dan as a product-formulating consultant. He overdelivered and brought much more depth than expected.” — June 17th., 2025
Zaq - Supplement Formula Optimization & Risk Assessment Consult
“Dan was highly professional and detailed with his work and recommendations. The consultation was extremely helpful and gave clear direction.” " — July 18th., 2025
Manik - Kids’ Gummy Supplement Formula Review + FDA Label & Amazon Compliance Consult
“Dan was knowledgeable, communicative, and provided valuable guidance during the early stages of our formulation review.” — December 16th., 2025
Kevin - Formulation Consult to Finalize Daily Brain Health Supplement for Adults 50+
“Dan consistently goes above and beyond. He is by far the most detail-oriented and responsive formulation expert I’ve worked with.” — November 4thth., 2025