Private label · Mārupe, Latvia · European Union
Private label food supplement manufacturer Europe
Food supplement manufacturer for private label needs. If you are medium or large size company and you looking for dietary supplement products for your private label.
100 000
tablets per hour on one machine
4
production lines: tablets & capsules, powders, effervescent, liquid forms
GMP + ISO + HACCP
certified manufacturing, EU standards
Contract manufacturing
Your brand. Our manufacturing.
Pharma Manufacture is a private label and contract manufacturer of food supplements based in Mārupe, Latvia, 2 minutes from Riga Airport. We produce tablets, capsules, softgels, effervescent tablets and sports nutrition powders for brands across the European Union in a GMP, ISO and HACCP certified facility. Brands start from 150 units with a lead time from four weeks, choose a ready-made (stock) formula from a catalogue of 350 or have one developed, and get label design, packing and EU compliance support. We specialize in working with medium and large size companies.

Tablets, capsules & softgels
Direct compression tablets, gelatin and vegan HPMC capsules, soft gelatin capsules — ready-made and custom formulas.

Sports nutrition
Proteins, creatine, amino acids and complexes — packed in jars or doypacks under your brand.
Facility at a glance
| Capability | Detail |
|---|---|
| Tablet output | up to 100,000 per hour (single machine) |
| Production lines | 4 — tablets & capsules, powders, effervescent, liquid forms |
| Certifications | GMP, HACCP, ISO 22000, US FDA registration |
| Location | Mārupe, Latvia (EU), 2 min from Riga Airport |
| Quality control | Every batch lab-tested; Certificate of Analysis; samples kept 3 years |
| Traceability | Manufacturing data stored 10 years |

Made in the EU
European Union production, GMP, ISO & HACCP certified, registered with the US FDA
All our food supplement tablets and capsules are manufactured in the European Union in a GMP certified factory. Production complies with all European standards — Regulation (EC) No 852/2004 on the hygiene of foodstuffs, (EU) No 1169/2011 on food information to consumers and (EC) No 1924/2006 on nutrition and health claims. Our formula is simple: high quality at a good B2B price. The machines this runs on are listed with their technical data on our equipment page.
Quality
Every batch laboratory tested
Our quality department makes sure products are manufactured, packaged, labeled and held to standards. Company workers are high-class professionals from the field of pharmaceutical manufacturing and are trained by GMP, ISO and HACCP rules. The team runs the testing program for raw materials, semi-finished and finished products; each product batch sample is kept for a minimum of three years, and products are only released after meeting all requirements. Quality control team is also responsible for the testing program of raw materials, sami-finished and finished products.

Simple process
How private labeling works
- Request a price listTell us the product or send your full list — we reply within 24 hours.
- Choose packingBottles, blisters, tubes, jars or zip-lock bags for your format.
- Label designOur designer prepares artwork based on your brand and market.
- Manufacturing & packingWe produce, pack and label your tablets, capsules or powders.
- DeliveryThe finished product is delivered to your warehouse, EU-wide.
Why partner with us
Built for EU private-label brands
Our food supplements are suitable for sale in pharmacies, health stores, online stores, supermarkets, Fitness clubs (Gyms) and retail shops. Our experience in health care industry will help to ensure that your private label product not only meets the needs of your customer, but will be a profitable venture for your business. PHARMA MANUFACTURE is the best partner to achieving this goal.
Made in the European Union
Tablets, capsules and powders produced to EU standards — high quality at a manufacturer’s price.
Minimum order from 150 units
150 units of a ready-made formula in tablets or capsules, so you can put a product on the shelf before committing to stock.
Ready-made & custom formulas
Choose from our stock formulas or develop your own with our in-house R&D team.
A-to-Z private labeling
Full service: formula, label design, packing, registration help and delivery.
Fast product launching
Fast new private label (finished) product launching — from formula selection to finished goods.
Registration support
We help register the goods in your country when required.
GMP / ISO / HACCP certified
Annual audits and certification keep production compliant and traceable.
Private Label design service
Our designer will develop a suitable label design for your target audience and market.
Packaging options
All the products have different options for private label packaging and Branding (different types of labels, bottles, jars, ziplock-bags, tubes). Packing options: Bottle, Blisters, Tubes, Jars, Zip-Lock bag. Any amount per pack. Logistics – We provide delivery services or you can pick up goods from our warehouse in Latvia.

Logistics & facility
A purpose-built, ultra-efficient site
Our manufacturing site in Mārupe, Latvia is purpose-built for food supplements: A+++ energy efficiency, advanced moisture-control and air-conditioning, four production lines (tablets & capsules, powders, effervescent, liquid forms) and a secure location in the Green Park industrial zone, 2 minutes from Riga Airport, has suitable roads for trucks and is not far from the Free Port of Riga (Sea port). The site has two entrance gates for cars and trucks, outdoor lighting, alarm systems, camera surveillance and electronic key-card access to the production area. The logistics and warehouse department is responsible for ensuring that handling, storage, preservation and delivery procedures are maintained to ensure that there are no adverse effects on components, raw materials, semi-finished products, bulk materials and finished products. FEFO stock rotation is in place and happens fully automatic due to our warehouse management system.
Operations
Sanitation, documentation & R&D
Sanitation on site
A pest-management program and standardized cleaning routines for every area; all cleaning products comply with GMP rules.
Documentation & traceability
All manufacturing data is stored for 10 years and full traceability is maintained through the whole supply chain. Administration is in charge of controlling, adjusting, reviewing, and approving documents. There is a registration audit program in place, and all records are kept on file for at least a year following the batch’s expiration date.
Research & development
An in-house R&D team of pharmacists, biochemists, dieticians and nutritionists develops new and existing products. The quality and security requirements of the food supplements are our greatest priority. Company is constantly works on research and development of existing and new products both for regular price lists and for custom requests from the customers.
Manufacturing site description
The building was constructed using only high-end materials and was designed for dietary supplements manufacturing, equipped with an air suction system, conditioning system, compressed air lines, optimal LED lighting, clean water and easy-to-clean surfaces. The site is also equipped with energy-saving smart LED sensor lights. Cleaning agents and any other hazardous chemicals are kept out of the production area. The manufacturing site is located in a safe industrial zone (Green Park) with two entrance gates for both cars and trucks and sufficient outdoor lighting; alarm systems and camera surveillance are used to secure the site, and only those who have electronic key cards can enter the production area.
Sanitation on site
A pest management program is in place at Pharma Manufacture site for mice, rats, birds, insects and other pests. This program’s upkeep is handled by an outside partner, who also performs frequent audits. Trash removal is handled by the building owner company — waste is sorted, and recyclable waste such as cardboard or plastic is sent for recycling. Every piece of industrial equipment and space is subject to a standard cleaning process, and every manufacturing area follows a regular cleaning routine specific to that location. All personnel are instructed about the utilization of the items that may be utilized, and a summary of those products is listed on the schedule. All cleaning products are in compliance with GMP rules.
Certificates & staff training
The company provides HACCP (Hazard Analysis Critical Control Point), GMP, safety, hygiene and on-the-job training for new employees. HACCP and hygiene training is conducted annually and assessed by a written exam. Pharma Manufacture undergoes a number of yearly audits and inspections from both customers and government, and each year is accredited by a certification authority for GMP, ISO and HACCP requirements.
Besides the compliance and implementation of industry laws, guidelines and specific requirements of customers, Pharma Manufacture seeks to optimize working conditions for its employees. The company is also concerned with energy saving and waste reduction and separation, as part of company policy.
Certified manufacturing
Good Manufacturing Practice & HACCP
Pharma Manufacture undergoes yearly audits and inspections from customers and government bodies, and is accredited each year for GMP, ISO and HACCP requirements. Production complies with EU regulations including (EC) No 852/2004, (EU) No 1169/2011, (EC) No 1924/2006, (EC) No 1881/2006 and (EC) No 1935/2004 on food-contact materials.




| Certificate | Certificate No. | Issued | Valid until | Certification body |
|---|---|---|---|---|
| GMP — Food Supplements Europe Guide to Good Manufacturing Practice (March 2014) | GMP-FS-01 | 28 April 2026 | 17 May 2027 | BM Certification SIA, Riga, Latvia — accredited by LATAK (No. S2-564, EN ISO/IEC 17021-1), IAF MLA member |
| HACCP — Regulation (EC) No 852/2004 on the hygiene of foodstuffs | HACCP-01 | 28 April 2026 | 17 May 2027 | |
| ISO 22000:2018 — Food safety management system | MSC-22-1384 | 8 January 2026 | 7 January 2029 |
Scope of all three certificates: manufacturing and packaging of food supplements (tablets, capsules, powders). Certificate holder: SIA Pharma Market Solutions, “Kargo k-1”, Mārupe, LV-2167, Latvia. First GMP certification 24 January 2020, first HACCP certification 3 May 2022; both are re-audited every year.

EU compliance
All food supplements we manufacture comply with the rules of production and marketing for dietary supplements valid in the European Union:
- Regulation (EC) No 852/2004 — hygiene of foodstuffs
- Regulation (EU) No 1169/2011 — food information to consumers
- Regulation (EC) No 1924/2006 — nutrition and health claims
- Regulation (EC) No 1881/2006 — contaminants in food
- Regulation (EC) No 396/2005 — pesticide residue levels
- Regulation (EC) No 999/2001 — control of transmissible spongiform encephalopathies
- Regulation (EC) No 1829/2003 — genetically modified food
- Regulation (EC) No 1830/2003 — traceability and labelling of GMOs
- Regulation (EC) No 1935/2004 — food-contact materials
Formulas & R&D
Dietary Supplement Formulas / Research and Development
Successful dietary supplements begin with strong, scientifically considered formulations. Our company combines market insight, scientific expertise, and practical manufacturing knowledge to create supplements that are both effective and commercially successful.
We offer a wide portfolio of ready-to-order formulas across multiple food supplement formats, including tablets, capsules, powders, effervescent tablets, and liquid products. These formulations have already been carefully developed and optimized, allowing our partners to bring products to market quickly without spending additional time and resources on formulation development. This enables our customers to focus on what matters most – building their brand and driving sales.
Our formulations are inspired by the most effective dietary supplements and the best-selling products currently available on the market. By carefully analyzing consumer demand, ingredient performance, and market trends, we develop products that are both highly functional and attractive to consumers. This approach helps ensure that the finished products are not only effective but also easier for our partners to position and sell successfully.
Innovation is also a key part of our development strategy. Our team continuously monitors global market trends, scientific research, and emerging ingredients in the health and wellness sector. Promising and innovative ingredients are regularly evaluated and incorporated into new formulations, allowing us to present our customers with fresh product concepts that reflect the latest developments in the supplement industry.
In addition to our ready-made formulas, we offer a dedicated Research and Development service for clients who wish to create unique or customized products. Our R&D team includes experienced pharmacists and nutrition specialists who help our clients to design formulas that match their specific vision, target audience, and market strategy.
For clients who already have their own formula, we also provide fast and efficient formula calculation, allowing us to quickly assess the feasibility of production and move the project forward without unnecessary delays.
By combining proven ready-to-launch formulas, continuous innovation, and professional R&D expertise, we provide our partners with the flexibility and support needed to successfully develop and expand their supplement product portfolio.
Frequently asked questions
Common questions about our contract manufacturing facility
Where is your supplement manufacturing facility located?
Our factory is in Mārupe, Latvia — a European Union member state — 2 minutes from Riga Airport in the Green Park industrial zone. All products manufactured here carry full EU origin and comply with EU food supplement regulations.
What certifications does your manufacturing facility hold?
The facility holds Good Manufacturing Practice (GMP), ISO 22000 and HACCP certificates, renewed through yearly audits and government inspections. Production also complies with EU Regulation (EC) No 852/2004 on food hygiene, (EU) No 1169/2011 on food labelling, and (EC) No 1924/2006 on nutrition and health claims, among others.
What is your production capacity for tablets and capsules?
Our facility runs four dedicated production lines and can produce up to 100,000 tablets per hour on a single tableting machine. The lines cover tablets and capsules, powders, and effervescent tablets independently.
Do you offer custom formula development, or only ready-made formulas?
We offer both. You can choose from our existing stock formulas for a faster launch, or work with our in-house R&D team — pharmacists, biochemists, dieticians and nutritionists — to develop a fully custom formulation for your brand.
How do you ensure traceability across the supply chain?
All manufacturing data is stored for 10 years and full traceability is maintained throughout the entire supply chain. Every finished product batch sample is retained for a minimum of three years, and products are released only after passing all quality requirements in our in-house laboratory.
Can you help register our supplement product in our country?
Yes. We provide registration support as part of our full A-to-Z private label service, helping brands navigate the notification or registration requirements applicable in their target EU market. Contact us to discuss the requirements for your specific country and product.
Request a price list for your private label
Tell us what you want to manufacture — tablets, capsules, softgels, effervescent or sports nutrition. We’ll send a price list and realistic lead times within 24 hours.
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