Custom supplement manufacturing
We formulate, manufacture, and test your custom supplement in one U.S. cGMP facility. Capsules, tablets, powders, and liquids, from small batch to full production.
Get a same day quote
Request received
A pharmaceutical scientist will review your project and reply the same business day.
- CertificationEurofins cGMP certified
- InspectionFDA inspected, no Form 483
- TeamPhD pharmaceutical scientists
Custom supplement manufacturing services
Nutraceutical contract manufacturing for capsules, tablets, powders, and liquids, formulated, manufactured, and tested by one technical team in one U.S. cGMP facility, with no outsourced testing, no middlemen, and no white-label shortcuts.
Capsules
Custom formulations in capsule form. Every batch tested for identity and potency.
Tablets
Immediate-release, enteric-coated, controlled-release, bilayer, and orally disintegrating.
Powders
Bulk, bottles, and sachets. Blended and tested under cGMP.
Liquids
Oral solutions and suspensions, in bulk or final packaging.
Supplement formulation services
Pharmaceutical scientists select ingredients and design the dosage form for your custom supplement.
Included- Ingredient selection and raw material sourcing
- Formulation development and optimisation
- Pilot batches before commercial runs
cGMP supplement manufacturing
Dietary supplement manufacturing in the U.S. under 21 CFR Part 111, with documented batch controls.
Included- FDA-registered facility in Elkridge, Maryland
- Pilot batch through to commercial volumes
- Bottling, labelling, and packaging
Analytical testing
Identity, potency, microbial, and heavy-metals testing in a PhD-staffed cGMP lab.
Included- Raw materials tested before manufacturing
- Analytical method development and validation
- Independent QA review of all testing data
A trusted dietary supplement manufacturer in the USA
Vici Health Sciences is a nutraceutical and custom supplement manufacturer run by pharmaceutical scientists. From an FDA-registered cGMP facility in Maryland, our team has developed more than 50 formulations, supported over 30 clinical trials, and taken 15 or more products through FDA ANDA approval. The co-founders, both pharmaceutical scientists, still run formulation and quality assurance. That is the standard your supplement is made to.
Capsules, tablets, powders, and liquids are formulated, manufactured, and tested under one roof. Every batch is checked in our own cGMP laboratory for identity, potency, microbial limits, and heavy metals, then released with a Certificate of Analysis. Your product is what the label says it is, batch after batch.
Where are you starting from?
- Formula ready: we manufacture and test it.
- Idea stage: we develop the formula, then make it.
- Existing product: we move it or reformulate it.
Small batch supplement manufacturing through to commercial volumes, with the same scientists in the same facility.
Raw materials
Identity and heavy-metals testing on every incoming ingredient before manufacturing begins.
In-process
Testing during manufacturing operations, so a batch that drifts is caught on the line, not after packaging.
Release
Identity, potency (assay), microbial limits, and heavy metals on the finished product, documented in a Certificate of Analysis.
Stability
ICH stability storage and testing to establish shelf life and support your label claims.
Methods
Analytical methods developed and validated in-house, so results are reliable and repeatable.
Quality assurance
Every result reviewed and approved by an independent QA department before a batch is released.
What to expect from Vici
Small batch supplement manufacturing with pilot batches from 250 units, commercial runs from around 3,000, a formula that stays yours, and every batch released by Quality Assurance with a Certificate of Analysis.
Made under cGMP with released ingredients, approved production records, and finished-product QC testing. Pilot units can be packaged and labelled for sale.
Where unit economics usually become feasible. Flexible by product, manufacturing process, and packaging.
Depending on the product and its technical challenges. You evaluate the prototypes for taste, texture, and mouthfeel.
The custom formulation, the label, and the brand belong to you, not to Vici: private label supplement manufacturing in the USA, built on a formula you own.
Sourced by Vici or supplied by you, then documented, identity tested, and released through cGMP procedures.
Deviation, out-of-specification, and corrective and preventive action systems find the cause and decide the disposition.
Projects that are a strong fit
- Differentiated supplements that need more than commodity manufacturing
- Products that need taste, mouthfeel, stability, blending, compression, or filling optimised
- A prototype or benchtop formula moving into controlled production
- Established brands that want a technically engaged U.S. partner and reliable supply
- Tablets, chewables, ODTs, capsules, powders, and liquid solutions or suspensions
Problems we fix before production
- Poor powder flow and ingredient segregation
- Inconsistent capsule fill
- Tablet capping, friability, and oversized tablets
- Unpleasant taste and mouthfeel
- Sedimentation and poor physical stability in liquids
Supplement manufacturing FAQs
Yes. Most clients engage Vici for formulation development. We develop a proprietary formulation around your ingredients, target dose, dosage form, sensory goals, claims, and cost targets.
Yes. We review existing formulations for ingredient suitability, manufacturability, stability, consumer experience, and scale-up requirements. A benchtop process may need adjustments to run reliably on production equipment, so we start with a feasibility and technical-transfer review.
Yes. Your custom formulation belongs to you. So do your label and your brand.
Yes. We source active and inactive ingredients from qualified suppliers, and can also accept client-provided ingredients provided they meet Vici's QA standards and applicable FDA regulations. Materials are received, documented, and released through cGMP quality procedures, including identity testing where required.
Typically 250 to 1,000 finished units, flexible by product, equipment, and packaging. A pilot batch bridges development and commercial production: it proves the formulation, the manufacturing process, packaging, labelling, and finished-product quality before a larger order is placed. Pilot batches are made under cGMP with released ingredients, approved production records, and finished-product QC testing.
Yes. Pilot units can be placed in supported commercial packaging with finished-product labels after the required quality review and release procedures.
Vici typically performs or coordinates identity, purity, microbial, and heavy-metals testing against the specifications approved for your product. Quality Assurance reviews the manufacturing documentation and test results before releasing the batch and issuing the finished-product Certificate of Analysis.
Yes. Vici is third-party dietary supplement cGMP certified by Eurofins and has been inspected by the FDA without receiving a Form 483.
Vici has formal deviation, out-of-specification investigation, and corrective and preventive action systems to investigate the issue, document its cause, and determine the appropriate disposition.
Unit economics generally become feasible at around 3,000 finished units. Vici stays flexible based on the product, manufacturing process, and packaging requirements.
Get a same day quote
Tell us what you are making and where you are starting from. A formulation specialist reviews your request and replies the same business day.
What happens next
- 1A pharmaceutical scientist reviews your product, format, quantity, and stage.
- 2You receive a quotation for pilot or commercial production, or a development proposal if the formula still needs work.
- 3Any foreseeable manufacturing or quality risk is flagged before a larger batch is committed.