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Small & Mid-Pharma Specialists

Custom Supplement Manufacturing Backed by Pharmaceutical Science

Formulation-led nutraceutical manufacturing in a U.S. cGMP facility - for established brands switching manufacturers, businesses adding a supplement line, and founders ready to scale.

cGMP Certified FDA Registered Maryland, USA 21 CFR Part 111

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Takes 30 seconds. A formulation specialist responds within 24 hours.

Unusual dosage form, or a one-off project like clinical supplies manufacturing? Choose Other and tell us what you need.

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A pharmaceutical scientist will review your project and respond within 1 business day.

Free, no commitment · Reviewed by a pharmaceutical scientist
Capabilities

Everything You Need Under One Roof

Ingredient sourcing, formulation, manufacturing, and quality testing - coordinated by one partner with clear accountability and no handoffs.

Custom Formulation Development

Our team of pharma-trained scientists works with you to develop the right formula - assessing ingredients, dosage forms, and target market from the start. We handle the science so you can focus on your brand.

cGMP-Certified Manufacturing

We manufacture in a U.S. FDA-registered, cGMP facility with the quality systems, documentation, and batch controls applied to your supplement product.

From Concept to Shelf

Ingredient sourcing, manufacturing, quality testing, and packaging coordination - all handled under one roof. One partner, clear accountability, no handoffs.

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100+
Pharmaceutical formulations developed
Why Choose Us

Why Supplement Brands Choose VICI

Most supplement manufacturers are just that - manufacturers. We're pharmaceutical scientists who apply drug-development rigour to every supplement we produce.

  • Scientist-Led Formulation Science

    Your formula is developed by PhD scientists and a team with 20+ years of experience in pharmaceutical and nutraceutical manufacturing.

  • FDA-Registered, cGMP-Certified Facility

    The same quality systems used for pharmaceutical manufacturing, applied to your supplement. Based in Maryland, USA.

  • Pilot Launch Batches Available

    With a clear path to commercial scale. We work with brands that are serious about quality. Commercial minimums apply.

  • Scientists Founded, Built and Run

    Formulation, manufacturing, and quality oversight are all led by the people who built this facility.

"We treat every supplement with the same precision we bring to pharmaceutical products - because your customers deserve it."

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Who We Work With

Built for Brands Serious About Scaling

From a first pilot batch to commercial production, we partner with operators ready to bring a high-quality product to market.

Established Supplement Brands

Switching manufacturers or adding new SKUs - without compromising on quality, documentation, or batch-to-batch consistency.

Businesses Adding a Supplement Line

Profitable operators extending into nutraceuticals with one accountable partner handling formulation through to packaging.

Founders Ready to Commercialise

Brands with real traction and a clear plan, moving from concept to shelf and scaling to commercial volume.

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The Process

How It Works

From your initial concept to a shelf-ready product - here's the journey.

1

Consultation & Product Scoping

Share your product concept or existing formula. We evaluate feasibility, discuss dosage form options, and build a clear project roadmap.

2

Formulation & Ingredient Sourcing

Our scientists develop or optimise your custom formula, source regulatory-compliant raw materials, and test every ingredient in-house.

3

cGMP Manufacturing & Quality Testing

Manufactured under strict cGMP systems. Every batch undergoes identity, potency, microbial, and heavy metals testing - documented and traceable.

4

Packaging & Delivery

From bottling and labelling to final packaging, your product leaves our facility shelf-ready. We handle the last mile so you can focus on selling.

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Built on Pharmaceutical Science. Trusted by Serious Supplement Brands Nationwide.

Our drug-development expertise is backed by a proven track record of scientific excellence, regulatory compliance, and successful clinical outcomes.

0
Formulations Developed
0
Clinical Trials Involved In
PhD
Scientists Founded, Built & Run
0
ANDAs Submitted & Approved
cGMP Current Good Manufacturing Practice - Dietary Supplements seal

Our Maryland facility operates in full compliance with 21 CFR Part 111 cGMP requirements for dietary supplement manufacturing. All batches are produced, tested, and documented to those standards.

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Questions

Frequently Asked Questions

Tablets (immediate-release, enteric-coated, controlled-release, bilayer, and orally disintegrating), capsules, oral liquids (bulk and final packaging), powders (bulk, bottles, and sachets), and buccal formulations are supported. If a specific dosage form is needed, contact us to confirm feasibility.
Yes. As per cGMP requirements, all raw materials undergo identification and heavy metals testing before manufacturing. Potency (assay) testing is performed on active ingredients for both raw materials and finished products. Our analytical lab is cGMP-certified, staffed by PhD scientists, and all testing data is reviewed and approved by an independent QA department. Clients can also provide their own Certificate of Analysis from a certified third-party lab.
Yes. Vici was founded by pharmaceutical scientists and specialises in formulation development, analytical testing, and small batch manufacturing. The team develops custom supplement formulations with quality built into every step - from ingredient selection through to final product testing.
Pilot launch batches are offered for qualified projects, with a clear path to commercial scale. Commercial minimums apply for ongoing production. Provide format and target volume for confirmation.
Yes. Established international contacts exist for sourcing high-quality, regulatory-compliant raw materials. Incoming ingredients can be tested in-house to certify all raw materials meet quality standards before manufacturing begins.
Product format, target order quantity, timeline, current stage (formula ready vs needs development), and any packaging preferences. The more provided upfront, the faster a clear path forward can be given.
No. Work spans founders at the early stage through to established brands scaling commercial supply. What matters is seriousness about quality and a clear product in mind.
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Start Your Project

Ready to Build a High-Quality Supplement Product?

Tell us what you're making and your target timeline - we'll respond within 1 business day with the next steps and a clear path forward.

  • Free - no cost, no commitment
  • Response within 24 hours
  • Reviewed by a pharmaceutical scientist
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