Formulation, manufacturing and regulatory support for dietary supplements, from Longford, Ireland. Discover More

Building a healthier future
through innovation

Manufacturing, filling, QP batch release and storage from Longford. GMP, HACCP and FSSC 22000 certified.

Ireland's dietary supplement manufacturer

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Manufactured in Ireland, shipped from Longford to distribution partners across Europe, Africa, the Middle East, South America and Asia. Discover More

Distributed in over 50 countries worldwide

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Bioreva Sciences · Longford, Ireland

Your full-service supplement partner in Ireland.

From first formulation to finished, shelf-ready product, Bioreva Sciences handles the full supplement lifecycle from the Irish midlands. GMP, HACCP and FSSC 22000 certified manufacturing, QP batch release, FSAI-compliant labelling and HSE-approved storage, all managed from Longford.

Tablets in production at our Longford facility Capsules ready for packing Finished product for a range of client sectors
Manufacturing
Tablets in production at our Longford facility

Manufacturing

We manufacture tablets, capsules and powders through our network of GMP, HACCP and FSSC 22000 certified production partners, managed from Longford. Pilot runs start at 10,000 units for new products, scaling to multi-million unit commercial batches for established ranges.

  • Tablets, hard & soft capsules, vegan (HPMC) & powders
  • In-process weight checks, hardness testing & dissolution verification
  • One contact from formulation through to finished product
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Capsules ready for packing

Packing

Your product leaves our Longford facility carrying your brand, not ours. We handle blister packing, bottle and tub filling, sachet filling, label printing and application, carton packing and palletisation. Every label is reviewed for FSAI compliance before production.

  • Blister, bottle, tub & sachet filling from Longford
  • Private-label artwork & FSAI-compliant labelling
  • Carton packing & shipment-ready palletisation
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Finished product for a range of client sectors

Sectors

We manufacture for brand owners across the nutraceutical and functional food space, from early-stage Irish start-ups to established sports nutrition and wellness brands scaling into the UK and EU. We also produce for private label distributors and retailers who need a reliable manufacturing partner behind their own range.

  • Nutraceutical & functional food brands
  • Sports nutrition & performance brands
  • Private label distributors & retailers
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Beyond manufacturing

The rest of the job, handled.

Brand launch, formula adaptation, regulatory paperwork and warehousing.
Have a product in mind? Talk to us about format, formulation and pricing.

How it works

From your first call to finished product.

Four steps from initial brief to dispatch. Most projects go from signed quote to first delivery in 10 to 14 weeks.

1

Brief & Quote

Tell us what you need. We review your brief, recommend a format and formulation route, and return a quote within five working days.
2

Formulation & Compliance

We develop or adapt your formula, run stability tests, source ingredients from approved suppliers, and prepare your FSAI notification and label artwork.
3

Production & QC

Your product is manufactured under GMP conditions with in-process quality checks. QP batch release clears it for sale in Ireland and the EU.

4

Pack & Dispatch

Filled, sealed, labelled and packed at our Longford facility. We dispatch to your warehouse, your distributor, or direct to your customers.

Built on quality, backed by rigorous manufacturing standards.

BioReva Sciences is a contract manufacturer for the nutraceutical and health supplement sectors, based in Longford, Ireland. We produce tablets, capsules and powders under one roof, from formulation through to pack and dispatch.

Our facility operates under GMP, HACCP and FSSC 22000 certified processes, with every batch released against full documentation and QP sign-off. That standard gives our partners the confidence to launch across Ireland, the UK, the EU and beyond.

Certified quality

Every batch. Every product. Every time.

Our Longford facility is certified to GMP, HACCP and FSSC 22000 standards, with every process audited to keep pace with EU and UK regulatory requirements. That gives our partners confidence when launching products across Ireland, the EU, the UK and beyond.

Ready to talk about your product?

Tell us what you need and we will come back with a plan, a timeline and a quote.

Your Questions Answered

Common Questions

What is the difference between private label and white label supplements?

Private label means you are taking one of our existing, proven formulations and putting your own brand and packaging on it, the fastest way to add a product to your range. White label works the same way but usually refers to a base formula that multiple brands can use, adapted slightly for each customer.

QP (Qualified Person) batch release is the regulatory sign off confirming a batch meets EU or UK standards before it can be placed on the market. We manage this as part of our regulatory support service, alongside FSAI notification and EFSA health claim compliance.

Our head office and packing operation is based in Longford, Ireland, with a regulatory and commercial office in Dublin. Our distribution presence extends across the EU, UK and overseas markets including South America, Africa, Asia and the Middle East.

Our partner facilities are GMP, HACCP and FSSC 22000 certified. We can confirm the exact certification relevant to your product on request.

Ireland is an EU member state, so products manufactured here have direct access to the European single market. Since Brexit, supplements manufactured in the UK require additional importation steps, a separate EU QP batch release and re-registration to be sold in the EU. Manufacturing in Ireland avoids all of that, while still being close enough to the UK to serve that market efficiently.

Our standard MOQ starts at 10,000 units, with some flexibility depending on formulation complexity and format.

A private label product using an existing formulation can be ready in 6 to 8 weeks. A bespoke formulation with stability testing typically takes 12 to 16 weeks from initial brief to first commercial batch, depending on complexity.