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About PharmaEurope
PharmaEurope is a private label and white label food supplement company. The company is PHARMA EUROPE SOLUTIONS 2023 SL, CIF B56533847, based in Marbella, Málaga, Spain. Production is in the European Union, at the plant in Mārupe, Latvia, operated by SIA Pharma Market Solutions — under the same ownership.
500 bottlesusual minimum, per product
from 100 unitssmaller first order
4 to 8 weeksapproval to delivery
ISO 22000certified EU plant
We say that in the first paragraph on purpose. A buyer choosing a contract manufacturer needs to know where the product is physically made and who holds the certificates, and finding out later is the most common reason a first enquiry stops.
The Spanish company was registered in 2023. The manufacturing behind it is not new: the group has been producing food supplements in the European Union for more than twenty years. Two legal entities in two countries is an ordinary structure in this industry — one company sells, another manufactures — and it says nothing about how long the people involved have been making product.
Who we are, in one table
Everything a buyer usually has to ask for twice.
| Company | PHARMA EUROPE SOLUTIONS 2023 SL |
| Registration | CIF B56533847 |
| Office | Marbella, Málaga, Spain |
| Production | Mārupe, Latvia, European Union |
| Certification | ISO 22000:2018, certificate MSC-22-1384, valid to 7 January 2029 · HACCP · Food Supplements Europe GMP guide |
| US FDA | Facility registration 13674831934, valid to 31 December 2026 |
| Standard run | From 500 bottles per product |
| First run | From 100 units |
| Production time | 4 to 8 weeks |
| Formats | Capsules · tablets · softgels · effervescent tablets · powders · sports nutrition |
What we actually do
We manufacture supplements that carry someone else’s name. A brand comes to us with a product idea or an existing specification; we produce it, pack it, document it and ship it, and the brand sells it.
A ready-made formula
A composition we already produce, which you take under your own label without any development work. More than 300 of them exist across capsules, tablets, softgels and effervescent tablets, and a selection is listed, with strengths, on the ready-made formulas page.
Your own formula
Developed from your brief or your written specification, produced only for you, and proved on a trial batch before the first production run.
The first route exists because most new brands do not need a new recipe. They need a product on a shelf, in a quantity they can afford to buy twice.
Who we are for
- A company launching its first supplement and buying a few hundred units, not 50,000.
- A brand adding a format it does not currently have.
- A retailer or a distributor putting its own name on a product it already sells.
- We are not the right supplier for a brand that needs a bespoke formula in industrial volume from day one — that is a different conversation with a different kind of factory.
Why we spell it out
The commercial contract is with PharmaEurope in Spain. The manufacturing, the certificates and the batch records belong to the plant in Mārupe, Latvia, run by SIA Pharma Market Solutions, which shares ownership with PharmaEurope.
The certificates on this site are issued to that Latvian company, because that is the site that was audited. Publishing a certificate issued to a company you never name is how manufacturers lose the buyers who check — so we name it.
What the certificates say
ISO 22000:2018, certificate MSC-22-1384, issued by BM Certification (Rīga), valid to 7 January 2029, accredited by LATAK under EN ISO/IEC 17021-1. Scope: manufacturing and packaging of food supplements (tablets, capsules, powders).
HACCP under Regulation (EC) 852/2004, and the Food Supplements Europe Guide to Good Manufacturing Practice for Manufacturers of Food Supplements.
The facility is registered with the US FDA, registration number 13674831934, valid to 31 December 2026. A registration is not an FDA approval or certification — the FDA does not certify supplement manufacturers, and any company that says it does is telling you something untrue.
What you get
Documentation with every batch, a label checked against Regulation (EU) 1169/2011 and Regulation (EC) 1924/2006 before it is printed, and the composition you need to notify the product in your own market. Supplements in the EU are notified, not approved: the company on the label files with its national authority — AESAN in Spain — and we provide what the filing needs.
Asked before the first email
Who am I buying from, and who makes the product?
Your contract is with PHARMA EUROPE SOLUTIONS 2023 SL in Marbella, Spain, while the product is manufactured and packed at the plant in Mārupe, Latvia, operated by SIA Pharma Market Solutions under the same ownership. The certificates are issued to the Latvian company, because that is the site the auditors inspect.
Is the product made in the European Union?
Yes — it is manufactured and packed in Mārupe, Latvia, which is a European Union member state, so the finished product is made inside the EU from blending through to packing. Both steps run at the same certified site under ISO 22000:2018 and HACCP, and the packing is inside the certified scope.
What certification does the manufacturing hold?
The plant in Mārupe holds ISO 22000:2018, certificate MSC-22-1384 issued by BM Certification and valid to 7 January 2029, covering the manufacturing and packaging of food supplements. It also works to HACCP under Regulation (EC) 852/2004 and the Food Supplements Europe GMP guide, and is registered with the US FDA under number 13674831934.
Are you FDA certified?
No supplement manufacturer is, because the US Food and Drug Administration does not certify or approve food supplement manufacturers at all. It registers food facilities, and the plant in Mārupe is registered under number 13674831934, valid to 31 December 2026, which is what allows it to ship food products to the United States.
What is the smallest order you take?
The standard run starts at 500 bottles per product, and first runs have been produced from 100 units. Production takes 4 to 8 weeks from approval of the formula and the label artwork. Ask with your own numbers, because the answer depends on the format and the pack rather than on a fixed rule.
Can you develop a formula, or only produce existing ones?
Both. More than 300 ready-made formulas are already developed and in production across capsules, tablets, softgels and effervescent tablets, and any of them can be taken under your own label. We also develop a formula from your brief or your written specification, and prove it on a trial batch before the first production run.
Start a conversation
Tell us the format, the active, the dose and how many units you need for the first run.
- 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