{"id":8008,"date":"2026-08-12T01:21:36","date_gmt":"2026-08-12T01:21:36","guid":{"rendered":"https:\/\/oralabx.com\/?page_id=8008"},"modified":"2026-10-25T13:59:48","modified_gmt":"2026-10-25T05:59:48","slug":"innovation","status":"publish","type":"page","link":"https:\/\/oralabx.com\/ru\/innovation\/","title":{"rendered":"\u0418\u043d\u043d\u043e\u0432\u0430\u0446\u0438\u0438"},"content":{"rendered":"\t\t
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INNOVATION<\/h1>\t\t\t\t<\/div>\n\t\t\t\t
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Development and manufacturing partner for external innovation in oral care<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

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ORALABX works with R&D, external innovation and partnership teams \u2014 from early technical assessment through prototype, evaluation and commercial supply.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t

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\n\t\t\t\t\t\t\t\t\tThis page is a non-confidential capability summary. No registration required.\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t
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Send us a non-confidential brief<\/a><\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Download Capability Summary (PDF)<\/a><\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t
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No form required.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Where we contribute<\/div>\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\t\t\t\t\tMost manufacturing partners are engaged after the specification is final. We are set up to be useful earlier than that.\t\t\t\t\t\t\t\t<\/div>\n\t\t
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01<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Before the specification is fixed<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Feasibility input on formats, actives and processing constraints, so that the specification is written against what can actually be manufactured and shipped.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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02<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Reformulation of an existing product<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Alcohol removal, preservative system changes, flavour and sensory rebuilding, cost-structure reconstruction, or transfer into a different format.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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03<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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New format development<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Taking a defined consumer occasion \u2014 travel, post-meal, away from the sink \u2014 and building the product, the dose and the pack around it.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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04<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Qualified commercial supply<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Taking an already-defined product into validated, documented and repeatable production.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Scope<\/div>\t\t\t\t<\/div>\n\t\t\t\t
\n\t\t\t\t\t\t\t\t\tClear boundaries save screening time. This is what we take on, and what we do not.\t\t\t\t\t\t\t\t<\/div>\n\t\t
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IN SCOPE<\/div>\t\t\t\t<\/div>\n\t\t
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Mouthwash and oral rinses<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Toothpaste and gels<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Breath sprays and oral mists<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Unit-dose sachets, stick packs and travel formats<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Alcohol-free and low-alcohol systems<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Mineral, zinc and xylitol systems<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Flavour and sensory reconstruction<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Cosmetic-pathway documentation support<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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OUT OF SCOPE<\/div>\t\t\t\t<\/div>\n\t\t
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US OTC drug products<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

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Ingredient or active discovery<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

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Standalone formulation licensing or IP transfer<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Devices, electronics and diagnostics<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

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Bulk liquid and semi-finished supply \u2014 we supply finished, packaged, export-ready goods only<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Own-brand products sold into our customers' markets<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Technical platforms<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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These are the areas where we hold working experience rather than general capability.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t

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Zinc Alcohol-Free Systems<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Zinc Citrate + Xylitol is the primary alcohol-free development direction. Zinc PCA is evaluated only when a defined project brief and target-market pathway support it.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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PAP Suspension Systems<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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PAP suspension development focuses on dispersion control, appearance, sensory balance, stability observation and packaging compatibility before commercial scale-up.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Controlled Low-Peroxide Systems<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Controlled low-peroxide development uses an established commercial formula route, with flavor adjustment and removal of non-essential flavor components evaluated without changing the core system.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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On-the-go formats and dosing<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Spray dosing and atomiser selection, single-use sachet and stick-pack filling, and travel pack sizes designed for use away from a sink.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Sensory and flavour reconstruction<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Flavour systems for high-humectant and alcohol-free bases, where a flavour that performs in a standard base will not transfer directly.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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How a project runs<\/div>\t\t\t\t<\/div>\n\t\t
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Concept and technical alignment<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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We confirm what is technically and commercially possible before development starts, including regulatory pathway, format limits and packaging constraints.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Formulation development<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Two to three directions are usually developed in parallel rather than one, so the decision is made on comparison.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Prototype sampling<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Prototype samples for internal evaluation, followed by a revision round against structured feedback.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Technical evaluation and optimisation<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Stability, compatibility and applicable third-party testing before any commitment to production.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Commercial scale-up<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Documented, repeatable manufacturing under our quality management system.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Technical assessment \u2192 prototype sampling \u2192 structured evaluation \u2192 10,000+ units per SKU commercial manufacturing when qualified.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t

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Development, testing and manufacturing stages can be scoped separately within a commercial development programme.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Quality, testing and documentation<\/div>\t\t\t\t<\/div>\n\t\t
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QUALITY FRAMEWORK<\/div>\t\t\t\t<\/div>\n\t\t
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Standard<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Applicable operation<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Verification<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO 9001<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Quality management system<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Certified<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO 14001<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Environmental management system<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Certified<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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ISO 22716<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Cosmetics good manufacturing practice<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Certified<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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GMPC<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Good manufacturing practice for cosmetics<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Certified<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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SMETA<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Ethical and social compliance<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Audited<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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FDA MoCRA<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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US cosmetic facility registration<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Registered<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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INTERNAL<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Incoming material inspection, in-process quality control, finished-product quality control, pH, microbiological testing, packaging compatibility, leak testing, and finished-product stability over 90 to 180 days.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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THIRD-PARTY<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Carried out at internationally accredited (ISO\/IEC 17025) laboratories, according to project requirements and applicable test methods.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t

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Test<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Standard<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Preservative efficacy<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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ISO 11930 \/ USP 51<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Microbial limits<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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USP 61<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Absence of specified microorganisms<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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USP 62<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Heavy metals<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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EC 1223\/2009 \/ USP 232<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Packaging migration<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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D0 and D28<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Project-Specific Third-Party Testing<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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QB\/T 2738, GB 15979 \u2014 S. mutans, P. gingivalis, F. nucleatum<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Whitening<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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ADA method<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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DOCUMENTATION AVAILABILITY<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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We state what documentation exists and at which stage it becomes available, rather than offering an undefined qualification pack.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t

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Document<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Stage available<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Availability<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Capability summary<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Published<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Direct download<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Certification names, scope and issuing bodies<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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On request<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Public<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Standard supplier documentation list<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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On request<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Public<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Certificate numbers and copies<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Supplier qualification<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Named recipient<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Manufacturer identity and facility qualification documents<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Under NDA, if the project proceeds<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Confidential<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Project-specific technical and test documentation<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Under NDA, project-specific<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Confidential<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Neutral laboratory evaluation samples<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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After technical discussion under NDA<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Confidential<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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IP, confidentiality and anonymity<\/div>\t\t\t\t<\/div>\n\t\t
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Ownership<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Project-specific formulation rights and exclusivity arrangements are agreed as part of the commercial programme. ORALABX retains its pre-existing technical know-how, development platforms, manufacturing methods and other background IP. Ownership boundaries are defined before development begins rather than assumed afterwards.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Confidentiality<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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We do not publish client names, brands or project details, including for completed work. Any case material on this site is anonymised.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Anonymous processes<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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We are used to working with intermediaries who cannot disclose the end client during screening, and we do not require disclosure in order to respond to a technical brief.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Manufacturing and scale<\/div>\t\t\t\t<\/div>\n\t\t
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Manufacturing<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Commercial mouthwash and breath spray production is executed by the designated Fujian production facility. Formula consulting, development support, sample execution, commercial manufacturing and document issuance are confirmed separately for each project.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Oral care capacity<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Liquid oral-care capacity is planned against qualified project scope. Toothpaste concepts are evaluated separately and require confirmation of the licensed manufacturing route before any production commitment.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Standard MOQ<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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10,000 units per SKU for qualified commercial production<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Lead time<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Approximately 45\u201360 calendar days after formula, packaging, artwork, deposit and production requirements are confirmed.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Export<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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North America is our largest export market, with additional supply to Europe and the UK, the Middle East and Australia.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t

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Supply form<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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Finished, packaged, export-ready goods only<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Filling and packing line, partner manufacturing base.<\/div>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t
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Send us a non-confidential brief<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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If you are screening partners for a defined need, a short written brief is enough to get a substantive answer. You do not need to identify your client, and no NDA is required for an initial discussion.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

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oem@oralabx.com<\/div>\t\t\t\t<\/div>\n\t\t\t\t
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We reply in writing within three business days, including when the answer is that the need falls outside our scope.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t

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