2,500
MINIMUM (per SKU, per order)
2,500 packages
Full-Scope CDMO Packaging Portfolio · Every Format, Every Fill
Blister Packaging, Enteric Capsules, and Multi-Format Contract Manufacturing.
IOC sp. z o.o. is the PIS-registered manufacturer of food supplements and cosmetics, with registered establishments. Project format and feasibility are assessed within the agreed written scope.
PUBLISHED MINIMUM ORDER QUANTITIES
2,500 to 500,000 packages. One SKU. One order.
Published minimum order quantities are set per SKU and per order. Project requirements and commercial terms are defined in the written scope.
500K
MAXIMUM (per SKU, per order)
500,000 packages
CAPABILITY MATRIX
Project-Specific Format Review
Project format and feasibility are assessed against the product specification, applicable requirements and agreed scope. IOC sp. z o.o. is the PIS-registered manufacturer of food supplements and cosmetics, with registered establishments.
CAPSULES
Hard · Softgel
BLISTERS
PVC/Alu · Alu/Alu
BOTTLES
HDPE · PET · Glass
DOYPACKS
4 configurations
SACHETS & STICKPACKS
5 formats
LIQUIDS
Syrup · Drops · RTD
PASTES
Oral delivery
DERMCOSMETICS
All formats above
MODIFICATIONS
V-notch · ECO · Batch
CUSTOM
Open Innovation
PACKAGING EXAMPLES
MOQ is expressed in units (capsules, sachets, bottles). The table below converts unit MOQ to finished-package count at the two most common pack sizes.
HOW PACKAGING IS SELECTED
How is dietary supplement packaging selected?
Dietary supplement packaging is selected around the product format and stability needs, the required protection characteristics, pack configuration and user experience, target-market labelling requirements, and production-volume and logistics constraints. The right packaging is specified for the product and market; it is not a generic catalogue choice.
MOQ REFERENCE TABLE
Every Format. Every Minimum. Every Package Example.
All MOQs are per individual unit (capsule, sachet, ml-unit). Packaging examples assume standard fill counts. Exact MOQ may be adjusted for validated MBR transfers — contact our technical team.
CAPSULES
Hard Capsules
Ideal for precise dosing and product stability. Cellulose or gelatin shell. Active ingredients at clinical-grade density.
MOQ
MOQ: 150,000 units
PACKAGING EXAMPLES
30-cap bottle → 5,000 bottles · 60-cap bottle → 2,500 bottles
Softgel Capsules
The optimal delivery system for oil-based and lipophilic compounds. Seamless shell, hermetic seal.
MOQ
MOQ: 300,000 units
PACKAGING EXAMPLES
30-cap bottle → 10,000 bottles · 60-cap bottle → 5,000 bottles
BLISTER PACKAGING
Pharmaceutical Blister (PVC/Alu · Alu/Alu)
IN-HOUSE LINEBlister packaging options for tablets, hard capsules, and softgels. Individual tamper-evident dose units with two laminate configurations: PVC/Aluminium (thermoform) for standard products, and Aluminium/Aluminium cold-form for moisture-sensitive active compounds.
MOQ
MOQ: established individually
TECHNICAL SPEC
PVC/Alu · Alu/Alu cold-form · tamper-evident · GMP-compliant
BOTTLES
HDPE / PET Bottles
Industry-standard white or coloured HDPE and PET bottles for capsules, tablets, and powders. Child-resistant (CR) or standard closure. Induction-seal and desiccant options available for moisture-sensitive formulations.
MOQ
MOQ: 2,500 bottles
TECHNICAL SPEC
CR or standard closure · induction seal · desiccant insert option
Amber / Clear Glass Bottles
Glass packaging options for light-sensitive and high-value formulations. Amber glass provides UV protection. Dropper, pump, or DIN28 closure configurations. Used for liquid supplements and other agreed product formats.
MOQ
MOQ: established individually
TECHNICAL SPEC
Amber / clear · dropper · pump · DIN28 closure
DOYPACKS — STANDING POUCHES
Standing pouches for powders, capsule refills, liquid supplements, and cosmetic refills. Four commercial configurations — all available from Olympia Biosciences.
Classic Doypack (Standard)
Fold-bottom standing pouch for stable vertical shelf display. Optimal for bulk powders (whey, collagen, electrolytes) and capsule refill packs. Maximum capacity up to 2.0 litres depending on product bulk density.
MOQ
MOQ: established individually
TECHNICAL SPEC
Max 2.0 L · powder · capsule · granule
Doypack with Zipper (Ziplock)
Standing pouch with resealable ziplock for multi-use products. Critical for metered-dose supplements (scooped powders) and capsule packs — moisture-barrier laminate preserves product stability after first opening.
MOQ
MOQ: established individually
TECHNICAL SPEC
Resealable ziplock · moisture-barrier laminate
Doypack with Spout
Purpose-built for liquid and semi-liquid products. Maximum 1,500 ml. Spout placement: central (top-centre) or side-corner angled. Closure: twist-off or flip-top. Applied to liquid vitamins, collagen drinks, and cosmetic refill formats.
MOQ
MOQ: established individually
TECHNICAL SPEC
Max 1,500 ml · centre or side spout · twist-off / flip-top
Doypack with Euro Hook / Handle
Modified top-seal: euro-slot cut for retail peg display, or ergonomic carry handle for heavy packs (500 g–2 kg). Combines standing format with point-of-sale and retail distribution readiness.
MOQ
MOQ: established individually
TECHNICAL SPEC
Euro slot or carry handle · POS / retail-ready
SACHETS & STICKPACKS
Our flagship flexible packaging segment — 20+ filling lines, covering the widest dimension and form range on the market.
Classic Sachets (Flat Pouches)
3- or 4-side heat-sealed flat sachets for single-serve supplement doses or cosmetic samples (creams, masks). Standard production workhorse for powder, liquid, and gel formats across nutraceutical and personal care.
MOQ
MOQ: 75,000 units
= 2,500 boxes of 30 or 1,250 boxes of 60. Special formats (e.g. larger than 7×10 cm): MOQ set per project, up to 300,000 units.
TECHNICAL SPEC
3- or 4-side seal · powder / liquid / gel
Stickpacks
Narrow, column-formed pouches from roll film — the dominant on-the-go format for vitamins, collagen, and minerals. Direct-consume or dissolve-in-water. Highest retail velocity format in the global supplement market.
MOQ
MOQ: 250,000 units
TECHNICAL SPEC
Column-form from roll · on-the-go · direct or dissolve
DUO / TRIO Pouches (Multi-Chamber)
Multi-chamber sachets joined by perforation for single-hand separation. Ideal for two-step cosmetic protocols (Phase 1: peel; Phase 2: mask) or supplement AM/PM split-dose packs with separate morning and evening formulations.
MOQ
MOQ: established individually
TECHNICAL SPEC
2–3 chambers · perforation separation · AM/PM split-dose
Shaped Sachets (Custom Die-Cut)
After full payment and acceptance, the rights to the formulation transfer to you in full.
MOQ
MOQ: established individually
TECHNICAL SPEC
After full payment and acceptance, the rights to the formulation transfer to you in full.
Wet Wipe Sachets
Sealed sachet containing non-woven fabric saturated with functional liquid. Available in mini format. Applications: make-up removal, self-tanning, exfoliating, refreshing. Cosmeceutical and nutraceutical variants both available.
MOQ
MOQ: established individually
TECHNICAL SPEC
Non-woven + liquid fill · mini format available
LIQUIDS
Syrups
Multi-flavour, multi-composition production lines. Ideal for paediatric and general wellness formulations.
MOQ
MOQ: 20,000 units
Drops
Concentrated liquid formulas for targeted health applications. High bioavailability.
MOQ
MOQ: 50,000 units
Functional Drinks
Functional beverages for active, health-conscious consumers. RTD or concentrate formats.
MOQ
MOQ: 50,000 units
PASTES
Oral Pastes
Specialised oral-delivery format for high-concentration active compounds requiring controlled release.
MOQ
MOQ: 20,000 units
FUNCTIONAL MODIFICATIONS
Applicable to any flexible format above.
V-Notch / Easy-Open
Edge tear notch enabling single-hand laminate opening without scissors. Standard upgrade for all flexible packaging formats.
Batch Marking (In-Line)
Best-before dates and batch/lot numbers applied directly to the seal during filling — GMP-compliant traceability under EU food labelling regulations.
ECO / Recyclable (Mono-Structure)
Any flexible format executed in single-material mono-structure laminates — 100% recyclable. Full R-cycle compliance documentation supplied on request.
REGISTERED ESTABLISHMENT & PROJECT SCOPE
Registered establishment and project-specific requirements
PIS-registered manufacturer of food supplements; production establishment registered with PIS in Gdynia, Poland (ul. Polska 20).
Cosmetic project requirements
PN-EN ISO 22716:2009 · GMP FOR COSMETICS
Cosmetic project requirements, applicable product rules and format options are assessed within the agreed written scope.
PRODUCT SPECIALISATION
Project-specific requirements are reviewed case by case.
Food, Dietary Supplements & FSMP
PN-EN ISO 22000:2018 · CODEX ALIMENTARIUS GMP/GHP/HACCP
IOC sp. z o.o. is the PIS-registered manufacturer of food supplements; its production establishment is registered with PIS in Gdynia, Poland (ul. Polska 20).
SOFTGEL FORMATS
Gelatin · HPMC
Gelatin and HPMC format options are scoped to project requirements.
CERTIFICATES & ACCREDITATIONS
Full Certification Matrix — Both Facilities — Valid Through 2029
PN-EN ISO/IEC 27001:2023-08
Intellectual Property & Data Security
Our ISO/IEC 27001-certified information security management system protects formulation and project data; confidentiality obligations are defined in the applicable agreement.
Cert. No: PG/IOC/2026/05/Eng · Valid to: 21.02.2029
PN-EN ISO 22000:2018
Quality-System Controls for FSMP & Supplements
ISO 22000:2018 is a food-safety management-system certification. Refer to the Legal Hub for current certificate scope and validity.
Cert. No: PG/IOC/2026/03/Eng · Valid to: 21.02.2029
CODEX ALIMENTARIUS – FAO/WHO
Production Rigour & Hygiene (GMP, GHP, HACCP)
Applicable quality controls, release testing and batch documentation are defined in the product specification and agreed manufacturing scope.
Cert. No: PG/IOC/2026/01/Eng · Valid to: 21.02.2029
PN-EN ISO 9001:2015
Full Repeatability & Traceability
Physicians and pharmacists expect standardisation. The ISO 9001 quality management system ensures every production batch has identical, repeatable parameters — enabling full traceability of every capsule or sachet, from raw material receipt to finished product.
Cert. No: PG/IOC/2026/02/Eng · Valid to: 21.02.2029
PN-EN ISO 22716:2009
Standards for Dermocosmetics — Facility I
ISO 22716 applies to cosmetics manufacturing. This certification does not describe food-supplement or FSMP manufacturing.
Cert. No: PG/IOC/2026/04/Eng · Valid to: 21.02.2029
INTERNAL STANDARD (FULLY IMPLEMENTED)
Corporate Social Responsibility (CSR) & ESG
Project-specific formulation, evidence, quality and manufacturing requirements are defined in the agreed scope.
Status: Implemented internal policy · B2B audit-ready
OPEN INNOVATION MANDATE
If it can be formulated, we manufacture it.
Innovation begins with a written review of the product concept, evidence, formulation requirements and requested format. Project feasibility and minimum order quantities are defined in the agreed scope.
One operational boundary: we do not operate bar or energy-bar extrusion lines. For every other format and formulation type, MOQ and production architecture are established individually through Paid Due Diligence. No number is published here because every formulation is different.
EXAMPLES OF NON-CATALOGUE MANDATES WE EXECUTE
Functional mushroom coffees · Liposomal liquid shot pouches · Adaptogen stickpacks · Multi-enzyme wet wipes · Cosmeceutical shaped sachets · Physician-grade collagen glass bottles · Two-phase AM/PM sachet packs · Nootropic RTD beverages
Frequently Asked Questions
How is MOQ calculated — per unit or per finished package?
MOQ is calculated per individual unit (capsule, sachet, bottle), not per finished package. For example: 150,000-capsule MOQ at 60 capsules per bottle = 2,500 finished bottles. At 30 per bottle = 5,000 bottles. Pack size directly multiplies your SKU count.
Why do softgels have a higher MOQ than hard capsules?
Analytical release is defined in the product specification and agreed scope.
What is the minimum order for a new formulation project?
The 2,500-package floor applies when you already have a validated formula and Master Batch Record (MBR). New formulation mandates require Paid Due Diligence first — we define the commercial volume range as part of the feasibility audit.
Can MOQ be negotiated for large-volume enterprise programs?
Yes. All MOQs are subject to negotiation for enterprise and PE-backed programs with defined annual volume commitments. Enter via Paid Due Diligence and we will structure a production agreement based on forecasted demand, not fixed minimums.
Do you manufacture dermcosmetics and cosmeceuticals?
Cosmetic project requirements, applicable product rules and format options are assessed within the agreed written scope.
I have an unconventional product idea. Can you manufacture it?
Project feasibility and minimum order quantities depend on format and are defined through the agreed written scope.
OPEN-SCOPE PRODUCTION MANDATE
No catalogue. No closed formulas. No fixed MOQs.
Every format listed is a starting point. If your concept doesn't map to a standard category — that is precisely what our Paid Due Diligence mandate resolves. We establish MOQ, feasibility, and production architecture individually for your specific formulation and packaging requirement. One exception: bars. Everything else is on the table.
RELATED INTELLIGENCE
Scale-Up CDMOManufacturing controls and analytical release are defined in the product specification and agreed scope.EXPLORE ›Softgel Contract ManufacturingGelatin and HPMC softgel formats for food supplementsEXPLORE ›Advanced Formulation Technology: Liposomal & EntericProject-specific formulation assessment, evidence review and regulatory pathway are defined in the agreed scope. Manufacturing arrangements and any external testing are confirmed per project.EXPLORE ›ISO 27001 Formula IP ProtectionYour MOQ, your MBR, your formula — all under ISO-certified information security governanceEXPLORE ›Request a written scoped quoteSubmit a written brief for MOQ clarification and project scopeEXPLORE ›
Strictly B2B / Educational R&D Disclaimer
The pharmacokinetic data, clinical references, and scientific literature referenced on this page are provided strictly for B2B formulation, educational, and R&D purposes for medical professionals, pharmacologists, and brand developers. Olympia Biosciences™ operates solely as a Contract Development and Manufacturing Organization (CDMO) and does not manufacture, market, or sell consumer end-products.
Global Regulatory & No Health Claims. Nothing on this page constitutes a health claim, medical claim, or disease-risk-reduction claim within the meaning of EU Regulation (EC) No 1924/2006, the U.S. Dietary Supplement Health and Education Act (DSHEA), or other global regulatory frameworks. These statements and raw data have not been evaluated by the Food and Drug Administration (FDA), European Food Safety Authority (EFSA), or Therapeutic Goods Administration (TGA). The raw active pharmaceutical ingredients (APIs) and formulations discussed are not intended to diagnose, treat, cure, or prevent any disease.
Client Responsibility. The B2B client who commissions a formulation from Olympia Biosciences™ is responsible for market-specific regulatory compliance, health claim authorisation, labelling and marketing of its finished product, as defined by the applicable agreement.