A new era in contract manufacturing of dietary supplements: lower MOQ and faster implementation from January 2025

Minimum Production in IOC

Minimum Amounts of Dietary Supplements You Can Order Us

Hard capsules

Hard capsules ensure precise dosing and stability of bulk raw materials, MOQ specified on 150 capsules, which allows for division into, for example, 2500 packs of 60 capsules.

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Soft gelatin capsules SoftGel

SoftGel - soft capsules are ideal for oils and other liquid substances that require MOQ 300 capsules, which translates into e.g. 000 packages of 10 capsules or 000 packages of 30 capsules.

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Sachets

  • Sachets (powder): 75 sachets (000 packs × 2 sachets)
  • Sachets (liquid): 250 sachets (approx. 000 packs × 8 sachets)
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    liquids

    Drops: concentrates for specific health needs, with MOQ 5 units. Syrups: we produce syrups in various flavors and compositions, with MOQ set at 20 units. Functional drinks: suitable for athletes and active people, with MOQ 50 units.

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    Other forms

    We also produce other, unique forms of dietary supplements upon request. The minimum order quantity is determined individually. Ask us for details.

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    Don't know what to choose? Call now and we will tell you which form of dietary supplement will be best for your project

    From January 2025 we are introducing revolutionary changes in contract manufacturing of dietary supplementsby combining lower minimum order quantities (MOQ) z even shorter lead time. Thanks to the expansion of our machinery park, we are able to offer flexible conditions for production hard capsules and sachets, both in the model Private LabelAnd full contract manufacturing. This innovation will allow you to enter the market more effectively, stand out from the competition and ensure positive experiences (UX) of your recipients.

    Why choose our contract manufacturing from 2025?

    1. Reduced MOQ
      Now you can start producing dietary supplements from just 1000 packages, which is a significant reduces the entry threshold and investment risk. For start-up companies, this is a great opportunity to test a new product, and for established brands, a chance to expand their offering faster.

    2. Shortened turnaround time
      The modernized machine park enables us even faster pace production of hard capsules and sachets, which translates into rapid product launch. You gain a competitive advantage by providing consumers with access to innovative supplements in a shorter time.

    3. Private Label Model and Full Contract Manufacturing

      • Private Label: Use ready-made recipes, labels and proven procedures, just add your branding.
      • Full contract production: Fully independent choose the composition, product form and packaging – we will take care of the implementation in line with your vision.

    4. High quality and safety standards
      We operate on the basis of GMP standards (Good Manufacturing Practice) and HACCP, guaranteeing reliable quality and compliance with legal regulations. This ensures your hard capsules and sachets will meet all requirements, and customers will gain confidence in the safety and effectiveness of the supplements.

    5. Global approach and positive UX
      We made sure that the entire ordering, communication and customer service process was intuitive i przyjazny. We offer support in various languages, help adapt the product to legal standards in other countries (including EFSA in the EU, FDA in the US), and provide a transparent online ordering path.

      • Simple order forms – quickly and without unnecessary formalities.
      • Regular status updates – full transparency at every stage of production.
      • Individual consulting – specialists will help you choose the right composition and packaging and answer all your questions.

    Ensure positive user experiences

    We bet on user experience both from the business client and the end user of dietary supplements. Thanks to the new possibilities:

    • You shorten time to market – you respond faster to trends and customer needs.
    • You limit financial risk – you order exactly the quantity you need.
    • You guarantee the highest quality – you use modern production lines and receive support from experts in the field of supplementation.

    Get started today!

    Whether you're just starting out in the creative world, own brand of dietary supplements, or you are planning to expand your current offer, our new contract manufacturing terms available from January 2025 will allow you to achieve your goals faster and cheaper.

    Choose professionalism, innovation and the highest safety standards.
    Contact us and see how we can help you realize your vision of dietary supplements in the form of hard capsules and sachets!

    The most important benefits in a nutshell

    • Lower MOQ – from 1000 packages
    • Lightning fast execution – thanks to the extensive machinery park
    • Flexibility – Private Label or fully customized contract manufacturing
    • Expert support – recipe and marketing consulting
    • Global standards – GMP, HACCP and compliance with regulations in various countries

    We encourage you to contact us to discuss the details and prepare an individual offer. Together we will create dietary supplements that will meet the expectations of your customers and provide them with exceptional experiences!

    VIP Fast-Track: Priority Technology Transfer

    This dedicated communication channel is reserved only for mature corporate projects, pharmacy chains and global brands transferring existing large-scale production to a medical hub IOC.

    The iron criterion for entry is to have a ready technological specification (Master Batch Record / BOM) and a planned volume of a one-time batch exceeding 1,000,000 pieces.

    • Your Privilege: You bypass the standard implementation queue and start-up audit fees (Zero R&D Fee).
    • Fast Track: Your specification goes directly to the Chief Technologist, and the Senior Key Account Manager immediately optimizes the Target Price in accordance with ISO 22000.

    ⚠️ IMPORTANT - SYSTEM VERIFICATION:
    Due to the automation of the Transfer Department processes, inquiries with volumes below 1 million pieces or projects requiring the development of a composition from scratch, sent via this form, are automatically rejected by the system without analysis and valuationIf your project involves a smaller starting scale, please select the dedicated tab. "Start-up / New Projects".

    Error: No contact form.

    Medical Innovation R&D Department (Evidence-Based Medicine)

    This project track is reserved only for doctors, clinics, investment funds and creators of elite premium brands whose absolute priority is scientific reliability and proven clinical effectiveness.

    W IOC We don't produce generic substitutes from mass catalogs. We act as your private research institute. We design proprietary, uncompromising matrices based on patented raw materials, and each dose is verified against the global scientific literature (DOI numbers required).

    • Medical Dossier: We create a complete Project Science Book for you, which provides a strong legal, medical, and marketing shield for your brand.
    • Intellectual Property (IP): The innovation we build becomes your asset. We provide the option of a full IP Buy-Out to your company's balance sheet.

    📌 PROJECT QUALIFICATION:
    Inquiries from this section go directly to the desks of our Research Team. If your primary business goal is to create a budget-friendly product and compete with the lowest price on e-commerce platforms (private label models), please select the tab. "Start-up / New Projects".

    Error: No contact form.

    Implementation Department: New Projects and Brand Scaling

    This project path was developed for investors, technology start-ups and developing brands that want to build their own portfolio based on rigorous quality standards (ISO 22000, ISO 27001) without yet having a ready-made large-scale specification (Master Batch Record).

    As a certified medical hub (CDMO), we base our architecture on large-scale industry standards. We treat each project as an individual innovation. This means we don't pursue low-cost, commoditized projects (so-called "off-the-shelf private label"), relying on optimized quality of base components.

    Financial Architecture and Engineering Requirements:

    • Research Process (Paid Discovery): Developing a proprietary product matrix from scratch and fully validating it to meet GIS/EFSA requirements is an independent engineering service for us. It requires a start-up budget allocation (CAPEX) of PLN 15,000 to PLN 35,000 net. This cost, within Technological Implementation Credit, is subject to full capitalization (deduction) when you order target mass production on our lines.
    • Supply Chain Security: By contracting the freshest, global raw materials while maintaining pharmaceutical rigor, we use a transparent tranche settlement model (50% / 25% / 25%), guaranteeing uncompromising quality of each produced batch.

    Operational recommendation of the Management Board: While respecting the capital and time of young business organizations, we understand that the early stages of startup projects may require drastic minimization of initial costs. If your current market strategy relies on competing on final price on e-commerce platforms, our regulatory standards may pose a disproportionate barrier to entry. In such cases, we respectfully recommend partnering with flexible contract bottlers who specialize in cost-optimization for smaller volumes.

    Error: No contact form.

    Error: No contact form.

    contract production of dietary supplements - Schematic representation of the stages of contract production of dietary supplements IOC, from the selection of raw materials to final quality tests.

    Stages of Contract Manufacturing of Dietary Supplements

    1. Consultations and Planning

      Collaboration begins with understanding the client's needs and discussing the product concept. Team IOC helps in developing the recipe and selecting appropriate ingredients.

    2. Formulation and Testing

      After determining the composition of the supplement, laboratory tests are carried out to ensure the effectiveness and safety of the product.

    3. Production

      Depending on the form of the supplement (soft capsules, hard capsules, liquids, sachets), the product is manufactured according to the highest quality standards.

    4. Packaging and Labeling

      Ready-made supplements are packed and labeled in accordance with legal requirements and customer preferences. IOC offers a variety of packaging options including blister packs, bottles and sachets.

    5. Registration and Market Introduction

      IOC helps in preparing the necessary documentation and registering the product with the appropriate authorities, enabling the legal introduction of supplements to the market.

    Polish manufacturer of supplements on request - quality IOC
    Detailed description of the production process

    Key Elements of Cooperation with IOC

    IOC, as the leading contract manufacturer dietary supplements, offers a wide range of services that stand out from the competition:

    • Experience: Over 15 years of experience in the production of custom dietary supplements.
    • Certifications: Possession of key quality certificates, including ISO 22000, GMP, HACCP.
    • Individual approach: Adapting the production process to the specific needs of the customer.
    • Innovation: Continuous investments in the development of technology and production processes.
    • No own brands: IOC does not have its own brands of supplements on the market. You can be sure that your brand is our only interest.
    Scheme of contract production of dietary supplements - Contract manufacturer of dietary supplements company IOC - contract production
    Get to know the actual production costs
    Forms of dietary supplements available in IOC along with a minimum order quantity
    More about contract manufacturing

    Examples of Services and Product Forms

    IOC offers a wide range of dietary supplement forms, including:

    how to produce a supplement?

    Contact us

    If you want to learn more about cooperation opportunities, visit home page IOC or contact directly for more information express quote.

    VIP Fast-Track: Priority Technology Transfer

    This dedicated communication channel is reserved only for mature corporate projects, pharmacy chains and global brands transferring existing large-scale production to a medical hub IOC.

    The iron criterion for entry is to have a ready technological specification (Master Batch Record / BOM) and a planned volume of a one-time batch exceeding 1,000,000 pieces.

    • Your Privilege: You bypass the standard implementation queue and start-up audit fees (Zero R&D Fee).
    • Fast Track: Your specification goes directly to the Chief Technologist, and the Senior Key Account Manager immediately optimizes the Target Price in accordance with ISO 22000.

    ⚠️ IMPORTANT - SYSTEM VERIFICATION:
    Due to the automation of the Transfer Department processes, inquiries with volumes below 1 million pieces or projects requiring the development of a composition from scratch, sent via this form, are automatically rejected by the system without analysis and valuationIf your project involves a smaller starting scale, please select the dedicated tab. "Start-up / New Projects".

    Error: No contact form.

    Medical Innovation R&D Department (Evidence-Based Medicine)

    This project track is reserved only for doctors, clinics, investment funds and creators of elite premium brands whose absolute priority is scientific reliability and proven clinical effectiveness.

    W IOC We don't produce generic substitutes from mass catalogs. We act as your private research institute. We design proprietary, uncompromising matrices based on patented raw materials, and each dose is verified against the global scientific literature (DOI numbers required).

    • Medical Dossier: We create a complete Project Science Book for you, which provides a strong legal, medical, and marketing shield for your brand.
    • Intellectual Property (IP): The innovation we build becomes your asset. We provide the option of a full IP Buy-Out to your company's balance sheet.

    📌 PROJECT QUALIFICATION:
    Inquiries from this section go directly to the desks of our Research Team. If your primary business goal is to create a budget-friendly product and compete with the lowest price on e-commerce platforms (private label models), please select the tab. "Start-up / New Projects".

    Error: No contact form.

    Implementation Department: New Projects and Brand Scaling

    This project path was developed for investors, technology start-ups and developing brands that want to build their own portfolio based on rigorous quality standards (ISO 22000, ISO 27001) without yet having a ready-made large-scale specification (Master Batch Record).

    As a certified medical hub (CDMO), we base our architecture on large-scale industry standards. We treat each project as an individual innovation. This means we don't pursue low-cost, commoditized projects (so-called "off-the-shelf private label"), relying on optimized quality of base components.

    Financial Architecture and Engineering Requirements:

    • Research Process (Paid Discovery): Developing a proprietary product matrix from scratch and fully validating it to meet GIS/EFSA requirements is an independent engineering service for us. It requires a start-up budget allocation (CAPEX) of PLN 15,000 to PLN 35,000 net. This cost, within Technological Implementation Credit, is subject to full capitalization (deduction) when you order target mass production on our lines.
    • Supply Chain Security: By contracting the freshest, global raw materials while maintaining pharmaceutical rigor, we use a transparent tranche settlement model (50% / 25% / 25%), guaranteeing uncompromising quality of each produced batch.

    Operational recommendation of the Management Board: While respecting the capital and time of young business organizations, we understand that the early stages of startup projects may require drastic minimization of initial costs. If your current market strategy relies on competing on final price on e-commerce platforms, our regulatory standards may pose a disproportionate barrier to entry. In such cases, we respectfully recommend partnering with flexible contract bottlers who specialize in cost-optimization for smaller volumes.

    Error: No contact form.

    Error: No contact form.

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