Who we manufacture for
Six kinds of buyer come to a contract manufacturer, and they are not solving the same problem. What changes between them is the minimum, the unit it is counted in, and the paperwork they will be asked for. Everything below is the same plant, the same certificates and the same batch record — SIA Pharma Market Solutions, Mārupe, Latvia.
Supplement manufacturing for ecommerce and Amazon sellers
Online sellers lose money on two things: a minimum that buries cash in stock, and a restock that arrives after the listing has gone quiet. A standard run here is 500 bottles per product, selected first runs have been produced from 100 units, and production is 4 to 8 weeks from the day the formula and the artwork are approved.
- 18-month minimum shelf life is stated on every specification, so a listing is not sitting on stock that expires mid-season
- Your label is checked against EU labelling law before it goes to print, which is where most marketplace takedowns start
- Certificate of Analysis and batch documents travel with the order, ready for a marketplace compliance request
- Reorders run against the same approved specification, so batch two is the same product as batch one
Supplement manufacturing for gyms, coaches and fitness brands
Sports products are counted in kilograms of finished blend, not in bottles, which changes the arithmetic completely. Sports nutrition and sachets start from 100 kg of blend and run from 4 weeks; plain powders start from 300 kg. One gym chain or one coach with an audience can carry that.
- Jars, pouches and sachets are filled, sealed and boxed at the same plant that makes the blend
- A ready-made formula can be adjusted — a dose raised or a component removed — when the order volume supports the reformulation
- Flavour and solubility are settled on a sample you actually taste before anything is manufactured
- Nothing on the label claims a physical effect that EU rules do not allow, and that is checked before print
Own-brand supplements for pharmacies, clinics and practitioners
A pharmacy shelf is judged on paperwork as much as on product. Capsules and tablets run from 500 bottles per product in 4 to 8 weeks, and every batch leaves the plant with its documentation. The site holds ISO 22000:2018, certificate MSC-22-1384, valid to 7 January 2029.
- Certificate of Analysis per batch, with the batch documents that a pharmacy inspection will ask to see
- Manufactured in the European Union — SIA Pharma Market Solutions, Mārupe, Latvia — and the certificates are issued to that site
- More than 300 ready-made formulas already in production, so a first own-brand line needs no development work
- The same specification can be repeated for years, which is what a repeat prescription line needs
Launching a first own-brand supplement line
A first product usually fails on cost before it fails on the market: development is paid for once, stock is paid for twice. Taking a formula that already exists removes the first cost entirely. More than 300 ready-made formulas are developed and in production, and any of them can carry your label.
- Selected first runs have been produced from 100 units, which is a test of the market rather than a warehouse
- Stock packaging — PET bottles, tubes, pouches — so nothing waits on a tooling order
- Start selling from 4 weeks, counted from the approved artwork
- No development time to pay for, because the formula and its documentation already exist
Extra capacity and a second source for established brands
A brand that already sells does not come looking for a catalogue. It comes because one supplier is a single point of failure, or because a product needs to exist that nobody else sells. Both are handled from your own specification, or from one written with you.
- Your own formula is proved on a trial batch before the first production run
- Softgels to your own formula start from 1,000,000 capsules; ready-made softgel formulas start from 500 pieces
- Syrups run from 100 litres, oils with vitamins from 20 litres
- Same certified site, same batch documentation as every other order — a second source is only useful if it is documented like the first
Brands selling outside the European Union
This is the part of the job that almost no manufacturer writes down, so brands find it out late. Inside the EU a food supplement is notified, not approved. Outside it, nothing carries over automatically: markets such as Morocco, Egypt and Kenya each register the product locally, through a holder or a technical representative established in that country.
- What we hand over: the specification, the full ingredient and allergen declaration, the Certificate of Analysis for the batch, and the site certificates with their numbers
- What the destination asks for on top is a local matter — a registration holder, a local representative, sometimes pre-shipment inspection — and it is held by the importer, not by the manufacturer
- “Made in the EU” is a selling point, not a shortcut through registration, and treating it as one is the mistake that costs a launch season
- Tell us the destination market at the enquiry stage, because it can change the label, the pack and the documents you will need
Frequently asked questions
Who does PharmaEurope manufacture for?
Ecommerce and marketplace sellers, gyms and fitness brands, pharmacies, clinics and practitioners, brands launching a first own-label product, established brands adding capacity or a second source, and brands selling outside the European Union.
What is the minimum order for a new brand?
A standard production run is 500 bottles per product for capsules and tablets. Selected first runs have been produced from 100 units. Powders start from 300 kg of finished blend, sports nutrition and sachets from 100 kg, syrups from 100 litres.
How long does a first order take?
Production is 4 to 8 weeks, counted from the moment both the formula and the artwork are approved. Effervescent tablets, sachets and sports nutrition run from 4 weeks. Nothing is manufactured and nothing is printed before those two signatures.
Do I need my own formula?
No. More than 300 ready-made formulas are already developed and in production, and any of them can carry your label without a day of development work. A ready formula can also be adjusted if the order volume supports the reformulation.
Which documents come with an order?
The Certificate of Analysis for your batch and the batch documentation, plus the site certificates: ISO 22000:2018 MSC-22-1384, GMP-FS-01, HACCP-01 and US FDA facility registration 13674831934. The label is checked against EU labelling rules before print.
Can you register my product in a market outside the EU?
No, and no manufacturer can. Registration abroad is held by a local entity — an importer, a registration holder or a technical representative in that country. We supply the specification, the analysis and the site certificates that the local filing is built on.
Get a quote for your quantity
Tell us the format, the active, the dose and how many units you need for the first run. You will get a price for that quantity and for a larger one, so you can see where the unit cost goes.
- Phone
- +34 637 48 95 63
- Office
- Calle Nuestra Señora de Gracia 7, Planta 2, puerta C
Marbella, Málaga, Spain - Production
- “Kargo k-1”, Mārupe, LV-2167, Latvia