Questions 41 answers

Every question buyers ask us, answered here

TS LAB d.o.o. is a contract manufacturer of dietary supplements in capsules in Komenda, Slovenia. What others tell you after you ask, we put on the page: capsules, quality and documents, price and minimum order quantity, logistics and how we work together.

Getting started

Getting started

What exactly do you manufacture?

Dietary supplements in capsules, tablets and powder form, made and packed in our own factory in Komenda, Slovenia. We lead with capsules and we promise on capsules, packed into jars, into blisters on two pharma quality blister lines, and into packs built for an Amazon listing. Tablets and powders are made here too, on our own tableting and powder filling lines, with tablets in jars and powders in jars, pouches and sticks. Softgels are made here too, on our own production, and are packed in jars only. Gummies and liquids are not part of our published range, so ask and we will tell you in the first reply whether we can source them or not.

Are you the factory, or do you subcontract production?
TS LAB operates its own production site at Obrtna cona Potok pri Komendi 14, 1218 Komenda, Slovenia, with capsule, jar-packaging and blister lines. Confirm the manufacturing scope for your product in the offer. Factory visits are by arrangement.
How fast do I get a price?

TS LAB states a written offer within 1 to 3 business days of receiving your formulation or idea, your target market and your preferred format. That offer states pricing, timelines, packaging options and the minimum order quantity for your product. Read that as time to offer, not as time to product.

What does TS LAB actually do?

TS LAB d.o.o. is a contract manufacturer of dietary supplements in capsules in Komenda, Slovenia. We fill, pack, release and ship capsules made to your formula and under your brand, from our own factory at one address inside the European Union.

How do I start, and what happens after I write?
Send your formula or idea, format, quantity range and target markets. You receive a written offer within 1 to 3 business days. Agree the product specification, development work, purchasing commitments and payment terms before authorising the next stage.
What do you need in the first email?

The ingredients and the dose per daily serving, the pack you want, the quantity range you are planning and the markets you sell in. If the product already exists, add the current label and the latest batch certificate of analysis, and the answer gets a lot more exact.

Can you take over a product I already sell?
Send your current label, specification and latest batch certificate of analysis. We assess the formula, materials, process and packaging before agreeing the transfer. Any adaptations belong in the specification you approve.
Do I have to be a big brand to work with you?

No, but every product has a minimum batch size, and for a small first run that number decides whether the project makes sense. The minimum for your product is in your offer, in writing, which is faster than guessing from a page.

Capsules

Capsules

Do you make anything other than capsules?

Yes. We lead with capsules and we promise on capsules, in jars, in blisters and in packs built for marketplaces. Tablets and powders are made here too, on our own tableting and powder filling lines, with tablets in jars and powders in jars, pouches and sticks. Softgels are made here too, on our own production, and are packed in jars only. Gummies and liquids are not part of our published range, so ask and we will tell you in the first reply whether we can source them or not.

How do you decide which capsule size my formula needs?

It is a density question, not a milligram question. The same dose fills a different volume depending on the raw material and the blend, so the blend decides the fill weight, the fill weight decides the capsule size, and the capsule size decides the jar and the carton.

How much active can one capsule hold?

It depends on the bulk density of your blend and on the excipients, not on the label dose alone. If the daily dose does not fit one capsule it becomes two per serving, which changes the pack, the price per day and the shelf presence, so it is worth checking before the artwork is set.

Are your capsules suitable for a vegan product?
A vegan product requires assessment of the shell, active ingredients, excipients and processing requirements together. Agree the full specification and any certification requirement before production. A vegan mark applies to its defined product scope.
Can you pack capsules in blisters as well as jars?

Yes. TS LAB states two pharmaceutical quality blister lines alongside its packaging lines, and blisters and jars are two different production routes chosen at specification, not a finishing decision at the end.

Can you supply filled capsules in bulk, without packing them?

Yes. For brands and contract packers with their own packing lines, we fill the capsules and supply them in bags, quoted per 1,000 capsules, with the batch documents agreed for your order. Your line packs and labels them. See bulk capsules.

Quality and documents

Quality and documents

What is a certificate of analysis?
A certificate of analysis, or COA, records results for an identified material or product lot. Read the lot reference, tests, methods, results and limits alongside the specification. A COA covers the tests it reports; other batch and traceability records have different roles.
Does a GMP certificate prove that my batch is correct?

No. GMP certification covers the site, its processes and its quality system. Evidence for an individual batch is the certificate of analysis for that batch, plus the specification it was released against.

Is there an official European Union GMP certificate for food supplements?

No. In the European Union a food supplement is a food, so the binding requirement is food hygiene law with HACCP under Regulation (EC) 852/2004, not the pharmaceutical GMP of EudraLex Volume 4. GMP certificates for supplement plants are issued by private certification bodies against published guidelines, most commonly the Food Supplements Europe guideline.

Is HACCP mandatory or voluntary?

The HACCP based procedure itself is mandatory for every food business operator in the European Union under Regulation (EC) 852/2004. Certification of that system by an external body is voluntary, and TS LAB states HACCP certification by Bureau Veritas.

Is TS LAB FDA approved?

No, and neither is any supplement manufacturer. The FDA does not approve dietary supplements or the facilities that make them. TS LAB states an FDA registered facility, which is a filing requirement under 21 CFR Part 1 Subpart H, and the FDA states that a registration number does not convey approval or endorsement of a facility or its products.

Do you hold IFS Food, BRCGS, ISO 22000 or FSSC 22000?

No. TS LAB states GMP, HACCP certified by Bureau Veritas, organic handling, FDA facility registration and V-CERT vegan certification. IFS Food and BRCGS are retailer driven standards normally required for supplying supermarket and drugstore own brands, and for direct to consumer, marketplace, distributor and practitioner channels the tested expectation is GMP, HACCP and documented traceability.

Can I check your organic certificate myself?

Yes, and this is the easiest of the five to verify. Organic handling is certified by KON-CERT Maribor under Regulation (EU) 2018/848, and the Slovenian Ministry of Agriculture runs a public search where a certificate can be found by certificate number or operator name and the document downloaded.

Can you make a health claim for my ingredient?
The wording, ingredient, dose and conditions of use must be assessed against the rules for your target market. For EU products, the EU Register of Nutrition and Health Claims is a starting point, not an approval of your finished label. Agree who reviews the claims and artwork before printing.
Pricing and MOQ

Pricing and MOQ

Why is there no price list on this site?

Because a price per capsule that is true for one project is false for the next one. The same capsule count can differ by a multiple depending on the purity of the active, the fill weight, the shell, the pack and the batch size. Your price comes in the written offer, within 1 to 3 business days of receiving your product details.

What drives the price of a capsule supplement the most?
The main drivers are the formulation, ingredient grades and quantities, shell, packaging, batch size and agreed testing. Their relative cost depends on your product. Compare offers using the same specification and scope.
What is MOQ and why does it exist?

MOQ, the minimum order quantity, is the smallest batch a given product can be produced in. It exists because a batch has fixed costs that do not shrink: line setup, cleaning between products, quality control and documentation are the same work for a small batch as for a large one.

Why can I be charged for raw material I did not use?

Because raw materials also have minimum order quantities. If the smallest quantity a supplier sells is larger than your batch needs, someone pays for the surplus. We tell you when that happens and whether moving up one batch tier costs you less than paying for material you leave behind.

What is overage?

Overage is the extra quantity of an active dosed above the label value so that the product still meets its label claim at the end of its shelf life. Some actives lose potency over time and need more of it, which is the honest reason two offers for the same label text can differ.

What is your minimum order quantity in units?
The minimum depends on the formulation, materials, production route and packaging. Send your intended order quantity and we will confirm the minimum and available quantity tiers in the written offer.
Logistics and markets

Logistics and markets

Where do you produce and ship from?

From one address, Obrtna cona Potok pri Komendi 14, 1218 Komenda, Slovenia. Production, packing, release and dispatch all happen at that site, inside the European Union.

How long does production take?
The production window depends on the approved specification, material and packaging availability, capacity and quality requirements. Your offer confirms the timing for your product. The 1 to 3 business day promise is the time to receive an offer, not the time to manufacture.
Which markets can you supply?
TS LAB manufactures in Slovenia for brands selling across Europe and beyond. Tell us the destination markets so the formula, label, documentation and any notification requirements can be assessed. Responsibilities depend on the product and supply arrangement.
Can you handle the notification of my product in my market?
Tell us the countries in which you plan to sell. Agree which documents TS LAB prepares, who reviews the product and label, and who files any required notification. Documentation support and filing are separate parts of the scope.
Can you run a rush reorder if a campaign sells out my stock?
For a repeat product, share stock cover, current sales and the date you need the goods. We assess materials, packaging and available capacity before confirming a production window. A faster reorder does not remove manufacturing, quality or release requirements.
Do you hold safety stock of packaging for repeat orders?
Ask about a material-stock arrangement for your repeat product. The components, quantities, ownership, storage terms and replenishment responsibility need to be agreed in writing; they are not automatically included with every order.
What forecast do you need from me to reserve capacity?
Share a rolling forecast by product, current stock, expected sales and the required arrival date. Update it when demand changes. A forecast supports planning; a production slot is confirmed separately against materials, capacity and the agreed order.
Can I sell the product on Amazon?
Requirements depend on the Amazon store, product and current request in your seller account. Check the compliance workflow, required testing, documents and deadlines for that listing. Share those requirements before agreeing the manufacturing and packaging scope; TS LAB cannot guarantee marketplace acceptance.
Working together

Working together

Who owns the formula we develop together?

Ask before you pay anything, with us or with anyone. Formula ownership belongs in the written agreement and not in the small print, and it is one of the questions we expect you to ask on the first call.

Can I visit the factory?

Yes. One production address inside the European Union means a customer audit is a short trip rather than an intercontinental project. Write to us with the dates that suit you and what you want to see.

Why are there no customer names or logos on this site?

Because we do not have written consent to publish them yet. A manufacturer's client list is the client's business, not ours, and inventing logos or testimonials is exactly the behaviour this site exists to avoid. Named references and case studies will be published as customers agree to them.

How do I know you will still be here in two years?

Look the company up. TS LAB, proizvodnja prehranskih dopolnil, d.o.o., registration number 6038573000, registered in Slovenia on 10 October 2011, credit rating AA+ for 2026 in the Companywall register, active, with no blocked accounts and no insolvency proceedings.

What happens if a batch does not match the sample I approved?

That is what the specification and the batch certificate of analysis are for. The batch is released against the specification you approved, and the certificate of analysis for the batch is the evidence you can put in front of a retailer, a platform or a laboratory.

What kind of project is not a fit for you?

Gummies and liquids, because they are not part of our published range. Ask and we will tell you in the first reply whether we can source them or not. Capsules, softgels, tablets and powders are all made here, and we lead with capsules. IFS Food and BRCGS are not listed in the materials reviewed for this website. If your buyer requires one, request confirmation of the current certified scope before proceeding.

Certificates

Which certificates does TS LAB state?

Five marks, each with the body behind it where the body is known, each on its own page with what it covers and what it does not cover. A badge without an issuer is worth nothing, so the issuer is named on the page, not only on the tile.

FDA registration is a filing, not FDA approval.

See all certificates and what each one proves

Question not answered here?

Write to us and get an offer within 1 to 3 business days, with pricing, quantity, packaging and timing for your product.

Registered company since 2011, credit rating AA+ (2026), registered data on the proof page.