Full Service

Supplement Manufacturer

57% Faster Turnaround Time Than Competition

In House R&D and

Formulation Specialists

Create, Improve, and Reverse-Engineer Any Supplement Formulation

cGMP, USDA Organic and

USDA Certified Facility

High Quality Products in a Fully Regulated Facility

Large And Small

Batch Capabilities

With the Most Competitive Prices in the Industry

Halal and Kosher

Supplement Certification

Ensuring Regulatory and Labeling Compliance

Industry Standard

Stringent Quality Control

Meeting Industry & Specialty Supplement Specification

Experienced Supplement Manufacturing Services

Vitalpax is a full turnkey manufacturing partner trusted by performance nutrition, health, and wellness brands in the U.S. and abroad. Whether you’re launching your first SKU or scaling a national line, our team brings deep expertise and market awareness to help you create high- quality supplements your customers will love.

Customized Supplement Development

Our in-house R&D team turns product ideas into commercially ready formulas – fast. Vitalpax specializes in custom manufacturing across capsules, tablets, softgels, liquids, and powders, with additional options like stick packs, sachets, gusseted bags, and bottle lines – all while targeting your channel strategy and regulatory needs.

Proven Manufacturing Process

Vitalpax operates under cGMP with rigorous quality systems from raw-material qualification through finished-goods release. Our in-house testing and QA/QC protocols help ensure identity, purity, potency, and microbiological safety – so you don’t have to worry about what’s hitting the shelf.

Pilot-to-scale under one roof: We support bench work through commercial production with high-speed encapsulation, tableting, and flexible packaging lines (bottles, jars, sticks, and sachets).
Innovation built in: Vitalpax tracks market signals and emerging ingredients, runs rapid formulation sprints, and validates stability and compliance in-house, so you can move on trend opportunities quickly without sacrificing quality or speed.

Our Certifications

Innovation to Execution: Our Proven Process

START

Ideation & Product Brief

We start with a collaborative working session to define the target customer, claims, delivery form (capsule, tablet, powder, liquid, stickpack, etc.), label targets, and channel needs. Vitalpax folds in market signals and ingredient intelligence so your concept is trend-right from day one. We also confirm regulatory guardrails and success metrics up front, then translate them into a concise product requirements document to guide R&D and operations.

FORMULA CREATION

In-House R&D & Custom Formulation

Our R&D chemists and formulation specialists turn your idea into a science-backed formula: creating new blends or reverse-engineering benchmarks as needed. We optimize actives, excipients, dosage forms, and shelf life while aligning to regulatory requirements and your go-to-market plan. Early on, we outline certification pathways (e.g., USDA Organic, Halal, Kosher, etc.) and ingredient sourcing options, balancing cost targets with performance and supply continuity.

TEST & VALIDATE

Prototyping & Lab Validation

Development prototypes move through comprehensive testing to protect integrity and accuracy. Using HPLC, FTIR, and other methods, we verify identity, potency, and compatibility through formulation, blending, and pilot runs – so what works on the bench also works on the line. We provide clear sample feedback loops and rapid iteration windows, keeping stakeholders aligned while we dial in performance and sensory attributes.

SCALE

Process Development & Pilot-to-Scale

We engineer for manufacturability – focusing on blend uniformity, flowability, compressibility, and stability. Whether you need small-batch customization or large-scale production, we de-risk scale-up and keep timelines tight. Documented process parameters and line trials reduce variability, and we establish final specs, sampling plans, and change-control procedures before commercial run.

PRODUCTION

cGMP Manufacturing with Full Traceability

Your product moves to cGMP production with seed-to-shelf traceability. High-speed encapsulation/tableting and flexible packaging (bottles, tubs, sticks, sachets, gusseted bags) deliver consistent quality for domestic and international markets. Every lot is tracked with batch records and CoAs; retains are archived for audits and post-market verification.

LAUNCHING YOUR PRODUCT

Launch-Ready Release & Fulfillment

This is where your product goes from “made” to market-ready.
QA/QC clears only lots that meet identity, purity, potency, and micro standards; labeling is verified, CoAs compiled, and export/retailer
paperwork finalized. We configure case packs, palletization, and
logistics (ASNs, lot coding) so you can ship immediately – arriving
shelf-ready for retail or DTC launch, complete with compliance
documentation and marketing assets aligned to your brief.

From Ingredients to Inbox

Vitalpax’s Oversight and Quality

Sourcing & Traceability

We qualify suppliers and document every lot from seed to shelf, prioritizing verified origins and consistent specifications. Full traceability ensures you (and your retailers) know exactly what’s in every batch.

Potency & Stability

We target label claims with calculated overages where appropriate and validate with time-point testing. Stability considerations (water activity, excipients, packaging) are built in to help maintain potency through shelf life.

In-House Testing & Release

Our control lab performs physical,analytical, and microbiological testingon raw materials and finished goods.Only lots meeting identity, purity,potency, and micro standards arereleased.

Certifications & Documentation

We operate under cGMP with retailer-ready documentation, including CoAs,batch records, and traceability logs.Certification pathways (e.g., USDAOrganic, Halal, Kosher, etc.) aresupported when applicable.

Fulfillment, Freight & Export

We handle case-pack specs,palletization, and compliant labelingfor domestic and internationalshipments. Shipping paperwork androuting guides are managed so yourproduct arrives shelf-ready.

Flexible Production & Storage

From small batches to national scale, we align production schedules, MOQs, and warehousing to your demand plan. Inventory rotation and FEFO practices help protect freshness and service levels.

Brand Registry, Listings & FBA Prep

We guide you through Amazon BrandRegistry, product setup, and FBApackaging/prep that meets strictinbound standards. Our goal is faster,cleaner onboarding with fewercompliance flags.

COA Compliance & Early Momentum

We produce recognized, accredited CoAs to meet Amazon’s supplement requirements and keep listings live . Launch support can include review-safe strategies and operational tweaks that help improve conversion and ranking over time.

Build Your Next Best-Seller

Launch faster with a turnkey partner – R&D, cGMP manufacturing, testing, packaging, and Amazon- ready docs all under one roof.

Explore Our Custom Supplement Contract Manufacturing Services

Get a Fast, Accurate Quote

Share your brief (dosage form, claims, volumes, timelines) and we’ll scope cost, lead time, and certification paths.

Frequently Asked Questions

1) What dosage forms can you manufacture?

Capsules, tablets, and powders are most common, with packaging options that include bottles, tubs & jars, and pouches (e.g., stick packs, sachets, gusseted pouches). Some projects also include liquids depending on scope and regulatory fit.

2) Do you offer custom formulations or only private label?

Both. We can develop a custom formula from your brief or provide ready-to-brand options that can be modified to your specification.

3) Who owns the formula if we do custom R&D?

For true custom development, you retain ownership of your formula once the project is completed and any development fees are settled. We maintain technical files for manufacturing and quality records only.

4) Can you reverse-engineer an existing product?

Yes—within regulatory and IP boundaries. We analyze label disclosures and use R&D best practices to create a functionally comparable formula.

5) What certifications and quality standards do you follow?

Manufacturing follows cGMP for dietary supplements with documented SOPs and batch records. Additional certification pathways (e.g., Organic, Kosher, Halal) may be supported depending on the project.

6) Will I receive Certificates of Analysis (CoAs)?

Yes. A finished-product CoA is issued per lot, reflecting the agreed specification and test results.

7) Can you help with label compliance and claims?

Yes. We review Supplement Facts, ingredient statements, and structure/function claims for U.S. dietary supplement regulations, and can flag items that may require legal or regulatory counsel.

8) What are your minimum order quantities (MOQs)?

MOQs vary by dosage form, packaging, and ingredient constraints. We’ll discuss practical starting volumes during scoping so the project is efficient and repeatable.

9) Do you support small batches or pilot runs?

Yes. Pilot or small-batch runs are available to de-risk scale-up, validate process parameters, and generate market test inventory.

10) What packaging options are available?

We support bottles, tubs & jars, and pouches (including stick packs, sachets, and gusseted pouches) plus retail cartons and compliant case-packing per routing guides.

11) How do we start a project?

Share your brief: target consumer, desired benefits/claims, dosage form, flavor (if applicable), certifications, volumes, and launch window. We’ll propose a scope covering formulation, testing, packaging, and production.

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