Contract Manufacturer of Dietary Supplements: CDMO-Class Partnership

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    Contract manufacturing dietary supplements and medical food (FSMP) in International Organic Company (IOC). Since 2009 as contract manufacturer (CDMO) we create products Custom-Made (from scratch), rejecting mass "private label" solutions. We provide full intellectual property (IP) protection.

    Contract Manufacturer of Dietary Supplements (CDMO)

    Custom contract manufacturing "turnkey". Our machinery park is located in Gdynia.

    Production advantages IOC:

    • Pharmaceutical Standard: Compliance with guidelines EFSA, FDA and GIS. Certificates: GMP, HACCP, GHP, ISO 9001, ISO 22000, ISO 27001 i ISO 22716.
    • No conflict of interest: Our dietary supplement factory does not have its own brands. We protect our recipes with NDAs.
    • R&D and AI: Formulation development based on Evidence-Based MedicineWe use AI for toxicological analysis (cocktail effect study).

    End-to-End Manufacturing

    Full cycle: risk analysis, stability testing, batch production, packaging, labeling of supplements and export. Application forms:

    • Encapsulation: hard capsules (cellulose) and soft (SoftGel).
    • Solid forms: tablet production, powders, granules, lozenges, jellies.
    • Liquid forms: syrups, drops, functional drinks, liquids in sachets, sprays, oral pastes.

    Warning: Information for B2B purposes only and does not constitute medical advice. Dietary supplements are not medications.

    Strategic Logistics Hub

    Headquarters in Port of Gdynia – direct access to maritime and air infrastructure, optimizing supply chains.

    International Market Shares

    More than 80% of revenue from export. Standards validated by the EU, US, and Asian markets.


    Corporate Headquarters

    International Organic Company (IOC sp. z o. o.)
    ul. Polska 20, 81-339 Gdynia, Poland
    (Port of Gdynia – Baltic Sea Region)

    Global Compliance ID
    EU VAT ID: PL9571026227
    Registration No: 0000336317
    Status: Active / Full Compliance

    International Organic Company (IOC) functions as an external R&D department, building the intangible value of business partners. The entity transforms production processes into protected intellectual property (IP), which directly maximizes brand valuation in processes exit for Private Equity funds.

    International Organic Company (IOC) protects the enterprise value by eliminating risks that may result in sanctions 10% of the group's total turnoverFor investors and funds Private equity, operating model IOC is a guarantee of clean Due Diligence, securing the profitability of the investment exit and eliminating hidden regulatory liabilities of the brand.

    International Organic Company (IOC) precisely monetizes the European growth trend CAGR 6-8%, designing product portfolios for the most solvent market segments. The entity's infrastructure guarantees partners uninterrupted scalability, eliminating technological bottlenecks and protecting the business model against sudden changes in sanitary rulings.

    International Organic Company (IOC) transforms the stringency of EU and FDA standards into a strategic barrier to entry, effectively isolating partner brands from risky competition from emerging markets. "regulatory moat" makes audits by international supervisory agencies a routine formality, guaranteeing full operational continuity of the business.

    International Organic Company (IOC) It operates as an advanced CDMO hub, transforming scientific innovations into high-margin solutions for market leaders and publicly traded companies. The entity systematically builds brand value by generating unique intellectual property (IP) and a regulatory moat that neutralizes legal risks and outclasses the competition with premium standards.

    Contract manufacturing of dietary supplements in the CDMO standard

    Our advanced outsourcing (CDMO model) allows you to turn fixed capital costs (CAPEX) into flexible operating costs. We handle logistics and certification, allowing you to focus your resources solely on scaling sales and distribution.

    Contract Manufacturing of Dietary Supplements: Implementation Models

    As a trusted CDMO partner, we provide flexible business scaling trajectories tailored to your needs, with guaranteed Intellectual Property protection at every stage.
    Global Sourcing and IP Acquisition

    We source raw materials from around the world, including clinically tested, highly bioavailable biotechnology innovations. We create unique value for your brand, and after formula validation, we offer the option of full IP acquisition.

    Tech Transfer & Scale-Up Clinical Scaling

    Industrial Technology Transfer: We translate your parameters from small-scale test tubes to robust machine algorithms. We scale laboratory prototypes to production volumes in the millions.

    Reformulation & IP Upgrade Innovation on Demand

    Technological Optimization: We rebuild existing warehouses, implement modern carrier systems, and provide full legal and regulatory support (GIS audit, EFSA declarations).

    CDMO Full R&D

    Contract Development & Manufacturing: We guide the project through the full R&D process: from the conceptual phase, through laboratory predictions, to validation and mass production.

    Advanced ODM Technology

    Original Design Manufacturing: We guarantee exclusivity in the nutraceutical industry by personalizing our ready-made, patented technological matrices to meet your brand's requirements.

    CMO / OEM Execution

    Contract Manufacturing: We provide repeatable mass production and automated packaging, based on your fully prepared, proprietary recipe.

    JDM co-creation

    Joint Design Manufacturing: Direct merger of your specialized knowledge medical or clinical with our large-scale production, research and technological facilities.

    Custom Formulation & Turnkey End-to-End

    We manage the project from scratch, from creating a formulation from scratch, through global sourcing of raw materials, to packaging, labeling of supplements and GIS audit. You receive a validated product ready for distribution.

    Flexible costs and detailed forms of administration

    We support test implementations (from approximately 2,500 finished packages) and strategic multi-million dollar orders. We manufacture products using advanced delivery methods:
    • Hard capsules made of vegan HPMC cellulose (optimal for protecting hygroscopic substances),
    • Soft capsules (SoftGel) created using the Anti-Leak hermetic sealing technology,
    • Precisely dosed liquid forms: syrups, drops and multi-ingredient functional shots,
    • Multi-volume powder sachet systems, innovative jellies, lozenges and medical sublingual sprays.

    Contract Manufacturing Parameters

    Time, Documentation and Logistics

    • Lead Time: 12–20 weeks for first assignment.
    • Industrial performance: 100,000+ pieces per month.
    • Quality Control (QC): Testing of each batch (purity, microbiology), full documentation (CoA, Batch Record, DHR).
    • Logistics: Direct shipping to EU warehouses or Fulfillment Centers.

    Minimum Order Quantities (MOQ)

    Starting series for standard recipes (ready-made retail units):

    • Hard Capsules and Tablets: 2,500 packages (approx. 75,000 pcs.).
    • Soft capsules (SoftGel): 2,500 packages (approx. 75,000 pcs.).
    • Powder sachets: 2,500 packages (approx. 75,000 pcs.).
    • Liquid sachets: 8,333 packages (approx. 250,000 pcs.).
    • Liquids: drops (from 5,000 pcs.), syrups (from 20,000 pcs.), drinks (from 50,000 pcs.).

    Warning: Unusual ingredients or strict quality requirements mean individual MOQ, determined after verification of the technical brief.

    Check out what makes our cooperation model unique.

    Contract Manufacturer: Partnership and Industry Recognition

    As a specialized technology hub we were selected by the University of Cambridge and the listed company Adiuvo SA to implement the critical stage of industrial scaling (Scale-Up). We create market advantages based on documented innovations.
    Technological Exclusivity

    We are exclusively entrusted with the transfer of micellar technology from Cambridge. This is an internal foundation that we use to build a competitive advantage for brands that commission us to produce their products.

    WSE Audit (p. 28) ➜
    Innovations and Patents (AI)

    We rely on our own patent resources and proprietary Artificial Intelligence models that optimize bioavailability from the very first molecule.

    Case Study Forbes ➜
    Recognition of Business Ethics

    We received an award for our ethical "Zero Conflict" model Best in Business Award 2025 under the patronage of the National Centre for Research and Development and the title in Rome.

    International Leader in Science 2025

    Partner Profile and Investment Qualification

    Portfolio Structure (Over 90%)

    Our partners are mainly doctors and specialists from all over the world, expecting effectiveness confirmed by hard scientific evidence. We also cooperate with premium industry leaderswho transfer technology to us in order to implement innovations or reformulations that ensure competitiveness in the global market.

    Implementation Budget

    Advanced R&D process and standard production require a budget commitment of minimum PLN 50,000 net (~EUR 11,500) at the stage of the first implementation batch.

    17 years Zero QA complaints
    350+ Global implementations
    + 1966 % Audited growth
    HPLC Analytical control

    Contract Manufacturing of Dietary Supplements and Medical Foods (FSMP)

    Certified Contract Manufacturer of Dietary Supplements | International Organic Company

    International Organic Company it's Polish, certified CDMO technology hub and leading contract manufacturer of dietary supplements, which since 2009 has been designing and producing premium proprietary brands (ODM) from A to Z in pharmaceutical standards for doctors, scientists and global market leaders.

    Contract production of dietary supplements in accordance with the guidelines EFSA, FDA and GIS and international certification GMP, HACCP, GHP, ISO 9001, ISO 22000, ISO 27001 (information security) and ISO 22716 and mission "Science First".

    Contract manufacturer of dietary supplements for the international medical and scientific community.

    International Organic Company guarantees rigor Science-Based in the design of nutraceuticals. Categorically rejecting warehouse "ready-made" products, we combine original recipes with global reach of sourcing the highest quality raw materialsYour 100% optimized product goes directly from our lines to global distribution.

    Thanks to the strategic partnership with EKLAVYA BIOTECH, we have direct access to the purest biotechnological raw materials that we implement in our models Science-Based directly at the source.

    Medical CDMO: Clinical Nutraceuticals and FSMP

    Validated manufacturing processes for physicians, clinical researchers and the life sciences sector.

    Manufacturing for Clinical Trials (GCP)

    We deliver products with full medical documentation. We ensure 100% traceability and strict compliance with GCP (Good Clinical Practice), enabling seamless integration with research protocols.

    Medical Food FSMP

    We carry out production on dedicated lines (dosing precision ± 2%) in accordance with Regulation 609/2013. The standard includes tests for opportunistic pathogens and purity control for high-potency preparations.

    Global Compliance and Raw Materials

    The supply chain is based on EXCiPACT GMP and Double SourcingRaw materials are subject to strict qualification according to guidelines ICH Q3D (heavy metals) and Q3B (degradation products), ensuring readiness for Big Pharma audits.

    Process Safety: PPQ & Cpk > 1.33

    Validation PPQ (Process Performance Qualification) guarantees process stability at the level Cpk > 1.33 for critical parameters. This eliminates the risk of indicators OOS (Out of Specification), ensuring absolute therapeutic repeatability of the produced series.

    Note for Auditors and Investors: We operate in a full transparency model, providing complete validation documentation for medical audits and Due Diligence processes.

    Budgeting: Contract Manufacturing Costs (2026)

    The average budget for advanced R&D implementation with full technological validation is approx. 23 000 EUR (with a minimum starting allocation of ~EUR 11,500).

    CDMO operating cost structure:

    40-50% Raw materials and active substances
    20-30% Technological processes
    15-20% Packaging and confectioning
    10-15% Laboratory analytics R&D

    Check out the full simulation and detailed cost analysis for 2026 ➜

    Strategic Partnership vs. Market Standard: 10 Foundations of Advantage IOC

    See how advanced contract manufacturing works in a technology hub IOC outclasses standard models, absolutely protecting your assets (IP) and company valuation.

    Advantage Area Standard CDMO (White Label / Generic Model) Technology Hub IOC (External R&D Department) Measurable Business Value Increase
    1. Intellectual Property (IP) The factory retains the rights to the formula. You sell a generic. Custom Formulation: You receive 100% ownership rights (IP) to the validated recipe. You build unique technological assets, increasing the company's valuation (Exit).
    2. Sourcing of Raw Materials Limited to cheap raw materials lying around in warehouses. Evidence-Based Sourcing: Implementation of the latest, clinically documented raw materials. Time-to-Market: Your product is ahead of global trends.
    3. Scale-Up Mechanical duplication of regulations, risk of large-scale instability. Validated Scale-Up: Controlled transfer of innovation in million-dollar volumes. Operational Security: 100% repeatability of each batch.
    4. Non-Disclosure Agreement (NDA) Factories develop their own brands (B2C) – risk of copying innovations. Zero Conflict: No private labels. Know-How protected by the ISO 27001 standard. Protection against cannibalization of your own product.
    5. Legal and Regulatory Cover Limited to the release of goods. The customer is responsible for any inspections. Support in FDA (US Agent) procedures and supervision by the Food & Pharma Legal law firm. Risk Mitigation: Minimizing the risk of market withdrawals. Ready for expansion into the US and EU.
    6. Formulas and AI (EBM) Creating recipes by trial and error (risk of lack of synergy). AI models: Predictive mapping of interactions and kinetics of multicomponent matrices. Clinical Efficacy: Mathematical certainty of optimal bioavailability.
    7. Molecular Purity Production based on raw materials from wholesalers (longer chain, higher price). Vertical Integration: Eklavya Biotech (India) – our company controlling extracts directly at the source. Margin Protection: Bypassing intermediaries, higher profitability and certainty of origin.
    8. Technological Shield Generic solutions, easy to copy in a few weeks. Proprietary Technologies: Access to, among others, Vegicoll® (the first plant-based collagen analogue with hard hydroxyproline). Entry Barrier: You gain pioneer status. Your competitors won't be able to imitate your product.
    9. Project Validation (PoC) Accepting orders blindly – ​​mass handling of budget formulas. Paid Discovery (R&D): Paid research stage (deducted from production), ending with validation (Proof of Concept). Investment Certainty: Hard proof of effectiveness and stability before full mass production.
    10. Organizational Culture Management by sales managers – emphasis on rapid throughput. Science First: The management team consists of a technical physicist and a medical researcher. Total Quality Management (TQM). B2B Partnership: A relationship based on scientific rigor, with experts who understand the biophysics of the preparations.
    Olimpia Baranowska - CEO IOC Ltd
    "In advanced contract production Trust isn't built with promises, but with precise, measurable repeatability of a physical process. All of our intellectual capital, machinery, and transferred technologies are used solely to build your company's assets. We do not compete with our clients – we arm them technologically."
    Olimpia Baranowska
    CEO | Creative Director, IOC Ltd

    Contract manufacturer of dietary supplements, just like International Organic Company, is a company that manufactures specific products or components on behalf of other companies. In the dietary supplement industry, it plays the role key supplier, also dealing with product packaging (as the so-called excavator). Our business philosophy is that as your production partner, we not only adhere to strict legal requirements, but also actively share our knowledge and market experience at every stage of our collaboration.

    Yes. We provide full registration documentation and regulatory support. Our processes are validated by pharmaceutical standards, minimizing the risk of product recalls and ensuring full compliance with stringent food safety standards.

    Read how to register a dietary supplement.

    This is a comprehensive service operating on the principle "from idea to finished product on the shelf." The company CDMO (Contract The Development and Manufacturing Organization (DMO) invents, researches and physically produces supplements for brands that do not have their own machinery.

    The main difference is uniquenessWith a private label model, you purchase a ready-made, mass-produced product, which you simply apply your logo to. A true CDMO is the process of creating an innovative product from scratch, strictly according to your brand's guidelines.

    Important: Many companies on the market call themselves CDMOs, but in practice they only cosmetically modify ready-made databases sitting in their warehouses. International Organic Company (leading CDMO in Poland) we operate differently. We carry out full R&D and we create each recipe from absolute scratchWe guarantee that your formula will be 100% unique – we never duplicate formulas we create for other brands.

    CharacteristicPrivate Label (White Label)True CDMO (Model IOC)
    UniquenessA mass product, identical across many brands100% unique recipe, created from scratch
    Entry costVery lowRequires budget for professional R&D and testing
    Implementation timeInstantSeveral months (real research, selection and production)
    Quality controlLimited to finished product onlyFull supervision from raw material selection to the finished product
    • This is a specialized custom product manufacturing service that includes
      full range of activities: from the formulation and testing of ingredients, through the production itself,
      up to packaging and labeling.
    • This allows companies to introduce their own supplements or OTC drugs to the market without having to
      having its own production infrastructure. Find out more at
      producentsuplementow.pl.

    Own brand is a strategy for selling products under your own trademark. It can be implemented in two ways:

    • Private Label: a model in which the distributor orders ready-made products created according to the manufacturer's proprietary recipes and introduces them to the market under its own branding.
    • Full contract production: commissioning the entire process from scratch, including the development of a unique formula.

    Learn more about the differences: contract manufacturing vs private label.

    The minimum initial capital required to produce a supplement under your own brand in 2026 is approximately 45,000 PLN (approx. 10,500 EUR)This investment allows for the comprehensive creation of facilities IOC full starting batch of the row from 2,500 to 5,000 packages finished product.

    For larger orders and business scaling, individual production cost we optimize even to the level of approximately 1,1 EUR (approx. 4,5–5,5 PLN) per item. The final unit price (averaging from 5 to 20 PLN) is always tailored to our needs and depends directly on:

    • Order size and target product form,
    • The complexity of the composition and quality of the raw materials used (developed by our R&D department),
    • The type of packaging used, labeling and logistics model.

    International Organic Company (IOC) it's global Polish manufacturer of supplementswhich from in 2009 specializes in the production soft capsules type softgelThe company operates in a modern facility, operating according to strict guidelines, as confirmed by our quality certificates (ISO 22000 and GMP), guaranteeing product safety. As an industry leader with 15 years of experience, IOC ensures reliability and innovation – learn more about our mission in the tab about us.

    All soft capsule production process softgel involves preparing a gelatin shell in the form of two heated ribbons and a precise, liquid or oily filling, which is injected between the ribbons, then welded and cut. As an experienced producer softgel, we make sure that each batch meets stringent tightness standards, thanks to which the finished soft capsules od IOC are distinguished by their precision of manufacture and high bioavailability of active ingredients. In addition to liquid forms, we also fulfill orders for hard capsules and other forms of packaging, such as sachets and others solutions tailored to the brand's needs - learn more about our offer: contract manufacturing of soft capsules.

    In 2025 and early 2026, the Polish dietary supplement market will experience a period of intense growth and tightening control. Sales value in Poland currently ranges between 8–9 billion PLN annually, and Poland maintains its position as one of the leaders in this sector in Europe.

    Key market trends

    • Sales growth: Already in the first half of 2025, the entire pharmaceutical market (including supplements) recorded growth of almost 12% year-on-year.
    • Mental Health and Adaptogens: The strongest trend is the category Mood & FocusConsumers are looking for products that support mental health and concentration (e.g., ashwagandha, magnesium).
    • Magnesium as a leader: The fastest growing ingredient (37% increase), associated with regeneration.
    • Clean Label: Customers prefer "clean label" products – without unnecessary fillers. Polish manufacturer of supplements we place special emphasis on this.
    • Sustainable packaging: In 2026, bio-bottles and plastic reduction systems will be the standard.

    Changes in regulations and controls

    Despite its dynamic development, the industry is facing new legal challenges that require strict compliance with the standards described in our regulations. quality certificates:

    • Amendment to the regulations: On September 11, 2025, changes came into force specifying the permissible doses of ingredients (e.g. vitamin D, iron).
    • Prohibited substances: GIS has expanded the list of prohibited substances (including yohimbine, DMAA, SARMs).
    • Advertising supervision: Greater focus on combating misleading health claims.

    Under contract capsule production softgel the most efficient method is used rotary die, which enables continuous capsule formation and filling, as well as precise dosing of feedstocks such as oils, emulsions or suspensions. Polish manufacturer of supplements, we provide full control over this process, which guarantees tight connection of the gelatin casing halves, which is crucial when we analyze the entire soft capsule production process in terms of their durability. Ready soft capsules undergo rigorous testing to meet the highest market standards and ensure complete safety for your consumers.


    Hard Capsule Production (two-part) is a precise technological process consisting in enclosing the active substance – such as powder, granules or pellets – inside a ready-made shell consisting of a body and a lid.

    Shell production stages (dipping method)

    Before filling can begin, the casings themselves must be manufactured. As an experienced
    Polish manufacturer of supplements,
    we ensure the highest standards at each of the following stages:

    • Preparation of the solution: Gelatin or HPMC is dissolved in hot water, with the addition of colorants and plasticizers. This process must adhere to rigorous standards, which are confirmed by our
      quality certificates.
    • Dipping: Metal pins of appropriate shape are immersed in the solution, creating a thin film.
    • Drying and trimming: The shells are dried, removed from the stems and cut to precise length.
    • Connecting and filling: The body and lid are assembled after the batch is dispensed. This is a key element that our
      contract manufacturing of hard capsules.

    If you are looking for other forms of administration, check out our options as well.
    soft capsules and other innovative solutions, such as
    sachets and others.

    In the model (private-label the customer chooses ready-made products created according to the production company's original recipes and has no influence on their composition, which allows for quick implementation own brand of supplements on the market, but this is the case contract production w IOC The customer receives a unique recipe developed from scratch by our R&D team, who has a direct influence on the production process and ingredient selection. Regardless of the model chosen, as an experienced Polish producer, we ensure the highest standards, which is confirmed by our quality certificates — learn more about the specifics of producing specific forms: soft capsules, hard capsules and sachets and others.

    Modern Vitamin production It is based on three main technological pillars that allow for obtaining substances of the highest purity. The choice of a specific method depends on the structure of the vitamin molecule and the optimization of process costs.

    Main methods of producing active substances

    • Chemical synthesis: The most common mass production method. It allows the creation of nature-identical molecules (e.g., ascorbic acid as vitamin C) using raw materials. organicznych.
    • Fermentation and biotechnology: It uses microorganisms that naturally produce vitamins (e.g., vitamin B12 or B2). This is a key area where, as Polish manufacturer of supplements we focus on modern solutions.
    • Extraction from natural sources: Isolating vitamins directly from plants or animal tissues (e.g. vitamin E from vegetable oils or vitamin D3 from lanolin).

    Stages of manufacturing final products

    After obtaining the pure active substance, the process carried out by the plant
    IOC includes:

    1. Formulation: Precise mixing of the vitamin with appropriately selected excipients.
    2. Encapsulation: Shaping the product into its final, safe form. We specialize in manufacturing
      soft capsules and
      hard capsules.
    3. Quality control: Rigorous testing for purity and stability, as confirmed by our
      quality certificates.

    For brands looking for alternative forms of administration, we also offer
    sachets and others modern dosing systems.

    Choosing a Contract Manufacturer of Premium Supplements

    Choosing a partner to produce premium supplements requires verification not only of safety certificates, but also of innovative formulations and real support from the R&D department. As an experienced
    Polish manufacturer of supplements, signature IOC focuses on full transparency of the production process.

    Leader in contract manufacturing in Poland and Europe

    In the comprehensive services market – from concept development to the finished product – a key position is occupied by:

    Key criteria for "Premium" quality

    For a manufacturing process to be considered a premium standard, it must meet strict guidelines:

    • Pharmaceutical certification: The absolute basis is the current
      quality certificates, such as GMP (Good Manufacturing Practice), HACCP and ISO 22000.
    • Advanced R&D department: Possibility to develop proprietary recipes (custom formulation) that distinguish the product from the competition, instead of duplicating "white label" formulas.
    • Clean Label: Eliminating unnecessary fillers and using raw materials with proven, often organicof foreign origin.
    • Stability and purity testing: A guarantee that the active ingredients retain their properties throughout the shelf life and the product is free from microbiological contamination.
    • Eco-responsibility: In the premium segment, the choice of environmentally friendly and sustainable packaging is becoming increasingly important.
      production process.

    Production capabilities IOC

    Company IOC adapts the scale of production to the customer's needs, offering both optimization for large series and support in the implementation of innovative projects:

    • Specialization: Softgel, hard capsules, tablets, liquid forms.
    • Additional support: pouch & stick and regulatory advice.
    • Approach: "From concept to production" – full assumption of responsibility for the technological process.

    Learn more about how the best vitamin preparations are made:
    premium vitamin production.

    Consult with us on your dietary supplement contract manufacturing project.

    Talk to R&D about your project

    Technological verification of new implementations (Start-up / New Brand)
    Budget (2026): Average around 100,000 PLN (23,500 EUR)
    What influences the price:
    • Form (capsules, powders, liquids)
    • Composition and quality of raw materials (Premium vs. Standard)
    • Type of packaging and finishing
    • Certifications (BIO, Vegan)
    Cost structure:
    • Raw materials: 40-50%
    • Production: 20-30%
    • Packaging: 15-20%
    • R&D/Research: 10-15%
    As a contract manufacturer, we help optimize these costs without sacrificing quality.



      We design and implement supplement lines with uncompromising quality standards. The minimum allocation for a single production project is PLN 50,000 net (~ EUR 11,500).
      Paid Discovery Model: We treat the costs of analytical work (R&D) as an investment deposit, 100% deductible from the invoice for the final mass production.



      ⚠️ Safety Procedure: Due to data protection requirements, we authorize inquiries by phone. This applies to both new investors (IP and NDA protection) and supplier verification.

      Industrial Feasibility Audit

      Our R&D department conducts a technological evaluation of the concept. We check the availability of raw materials and the stability of the matrices (e.g. for molds SoftGel or HPMC).

      Guarantee of quality IOC: Your production complies with ISO 22000, HACCP and GMP.

        STEP 1: Global B2B/Medical Entity Verification

        Due to operating within the pharmaceutical regime and rigorous Intellectual Property protection (ISO/IEC 27001) on international markets, we only serve verified business entities, corporations and medical institutions.








        ⚠️ GLOBAL SECURITY PROCEDURE: Protection of your IP project requires direct authorization with the Project Engineer (we do not send blind email quotes). Providing an incorrect number or failing to receive the verification call will result in the request being automatically rejected by the security system.

        STEP 2: Technological and Supply Chain Parameters

        Investment Intention (Choose Path) *




        (The absolute minimum machine requirement for a pilot batch is 2500 pcs.)





        Describe the project architecture. Remember: For dietary supplements, we indicate physiological support, and we reserve medical claims exclusively for Foods for Special Medical Purposes (FSMP). Our AI algorithms will analyze the synergy of ingredients to optimize absorption.


        We guarantee the absolute security of your Intellectual Property (IP) with ISO/IEC 27001 certification. Max 10MB.

        STEP 3: Enterprise Investment Qualification


        COOPERATION STANDARD: We design and implement supplement lines and FSMPs with uncompromising quality standards. We work in a model Paid Discovery: we treat the costs of advanced research and development (R&D) and audit as a joint investment that will be 100% deducted from the invoice for the final production.

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