Full Service Supplement Manufacturer
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.
- 57% Faster Turnaround TimeThan Competition
- In House R&D and Formulation SpecialistsCreate, Improve, and Reverse-Engineer Any Supplement Formulation
- cGMP, USDA Organic and USDA Certified FacilityHigh Quality Products in a Fully Regulated Facility
- Large And Small Batch CapabilitiesWith the Most Competitive Prices in the Industry
- Halal and Kosher Supplement CertificationEnsuring Regulatory and Labeling Compliance
- Industry Standard Stringent Quality ControlMeeting Industry & Specialty Supplement Specification
R&D, formulation and manufacturing
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.
Quality you can show retailers
View all certifications Our Certifications
Launching your product
Innovation to Execution: Our Proven Process
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.
Vitalpax’s Oversight and Quality
From Ingredients to Inbox
01Raw Materials
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.
02Quality Control
In-House Testing & Release
Our control lab performs physical, analytical, and microbiological testing on raw materials and finished goods. Only lots meeting identity, purity, potency, and micro standards are released.
Certifications & Documentation
We operate under cGMP with retailer-ready documentation, including CoAs, batch records, and traceability logs. Certification pathways (e.g., USDA Organic, Halal, Kosher, etc.) are supported when applicable.
03Logistics
Fulfillment, Freight & Export
We handle case-pack specs, palletization, and compliant labeling for domestic and international shipments. Shipping paperwork and routing guides are managed so your product 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.
04Amazon Expertise
Brand Registry, Listings & FBA Prep
We guide you through Amazon Brand Registry, product setup, and FBA packaging/prep that meets strict inbound standards. Our goal is faster, cleaner onboarding with fewer compliance 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.
Turnkey partner
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.
or call +1 866 848 2588
What we make
See all capabilities Explore Our Custom Supplement Contract Manufacturing Services
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.
Request a quote
Get a Fast, Accurate Quote
Share your brief (dosage form, claims, volumes, timelines) and we’ll scope cost, lead time, and certification paths.
or call +1 866 848 2588