CORE SERVICES

I provide high-quality solutions to help your business grow

01. Formulation & Product Development:

(New Products + Existing Formula Optimization)

The problem

Most supplements fail because:
• Ingredients are chosen for marketing, not science
• Doses are too low to be effective
• Extracts are poorly standardized
• Bioavailability is ignored
• Compliance is checked too late

What I do

I develop and optimize supplement formulations based on:
• Human physiology and mechanism of action
• Peer-reviewed studies and clinical data
• Real-world manufacturing feasibility
• Regulatory constraints of your target market

product formulation and development in laboratory

Two ways I help:

A) From Scratch New Product Development

If you have an idea like:
“I want a joint support / heart health / skin / sleep / energy supplement”
I will:
• Study the health condition and physiology
• Select ingredients with real scientific evidence
• Choose effective and safe dosages
• Decide the right dosage form (capsule, powder, liquid, gummy)
• Ensure ingredients are allowed in your target market

B) Optimization Existing Formula Review

If you already have a product, I:
• Review ingredient quality and extract strength
• Identify under-dosed or ineffective components
• Recommend better forms (e.g., standardized extracts, bioavailable forms)
• Improve efficacy without unnecessary cost inflation
• Flag compliance risks early
(Example: curcumin vs turmeric extract, extract standardization, bioavailability strategies, etc.)

developing product formula in research laboratory

You receive

• Clear formulation strategy
• Ingredient selection with reasoning
• Dose justification
• Optimization recommendations
• Manufacturer-ready formulation sheet

developing product formula in research laboratory

02. Regulatory & Label Compliance Support:

The problem

Products get flagged because:
• Ingredients fall under drug classification
• Claims cross regulatory boundaries
• Labels miss required statements
• Market-specific rules are ignored

What I do

I help you avoid costly mistakes by:
• Reviewing ingredient compliance per region
• Identifying ingredients that are restricted or prohibited
• Advising on what you can and cannot claim
• Structuring compliant Supplement Facts / Nutrition Panels
• Helping fix products flagged by Amazon or regulatory authorities

Markets covered

• USA (FDA / DSHEA)
• UK
• European Union
• Australia (TGA-aware support)
• Canada (supportive guidance)

You receive

• Ingredient compliance assessment
• Claims risk guidance
• Label structure recommendations
• Practical, fix-focused advice

product label compliance verification process
product label compliance verification process

03. Ingredient, Packaging & Product Sourcing:

The problem

Most brands struggle with:
• Unverified suppliers
• Fake or inconsistent COAs
• Hidden quality issues
• Poor communication with manufacturers

What I do

I source raw materials, finished products, and packaging through a trusted global network.

Sourcing regions

USA · Europe · China · India · Pakistan · Asia (Word Map with Countries colored)

What I can source

• Raw materials (extracts, actives, vitamins, minerals)
• Finished supplements (capsules, powders, liquids)
• Packaging (bottles, pouches, labels, scoops)

sourcing raw materials and packaging from suppliers

You receive

• Supplier shortlists
• COA and specification review
• MOQ and lead-time clarity
• Practical sourcing recommendations

sourcing raw materials and packaging from suppliers

04. Third-Party Lab Testing & Certification:

The problem

Many supplement brands struggle with:
• Amazon requests for lab reports or COAs
• Inconsistent or unreliable supplier testing
• Retailers demanding third-party verification
• Questions around potency, purity, or contamination
• Lack of credibility with consumers and partners

What I do

I coordinate independent third-party laboratory testing to verify that your supplement:
• Contains what the label claims
• Meets potency specifications
• Is free from contaminants and adulterants
• Aligns with regulatory and marketplace expectations

I work with globally recognized, accredited laboratories and manage the process end-to-end — from
sample submission to final reports. 


Types of testing supported:

• Identity & potency testing
• Heavy metals (Pb, Cd, Hg, As)
• Microbial testing (TPC, yeast, mold, pathogens)
• Pesticides & residual solvents
• Adulterant screening (where applicable)

When this service is used:

• Pre-launch verification
• Amazon or marketplace compliance requests
• Retail onboarding requirements
• Reformulation or supplier change validation
• Ongoing quality assurance programs

You receive

• Independent lab reports / certificates
• Clear interpretation of results
• Guidance on corrective actions if needed
• Documentation suitable for Amazon, retailers, or partners

laboratory technician performing product quality testing
laboratory test

05. Manufacturing & Scale-Up Support:

The problem

Good formulas fail during manufacturing because:
• Specs are unclear
• Manufacturers interpret formulas differently
• Scale-up changes product performance

What I do

• Prepare manufacturer-ready documentation
• Coordinate with your chosen manufacturer or co-packer
• Support pilot and early production runs
• Ensure formula integrity during scale-up

You receive

• BOM and master formula
• Manufacturing briefing pack
• Reduced back-and-forth with factories

factory production line for manufacturing scale up

06. Logistics to 3PL or Amazon FBA:

The problem

The final stage often breaks down due to:
 Packaging or label mismatches
• Incomplete documentation
• Poor coordination

What I do

• Support product handoff to your 3PL or Amazon warehouse
• Ensure packaging, labeling, and shipment readiness
• Reduce delays at the final step before launch

3PL warehouse handling Amazon FBA order fulfillment
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