BEMETICA
We are looking for a serious manufacturing partner able to support not only production, but also the technical, regulatory and documentary side required to launch a dermocosmetic product correctly in Europe.
Dermocosmetic manufacturer with formulation and regulatory support
The ideal partner is a manufacturer experienced in sensitive skin and dermocosmetic products, able to handle small initial production, guide formula adaptation if needed, and support the documentation package required for EU market launch.
Type of factory and capabilities required
- Experience in dermocosmetics, especially sensitive, reactive or redness-prone skin products.
- Ability to produce small initial batches with realistic MOQ options.
- Support for custom formula development, formula adjustment or adaptation based on available raw materials.
- Experience with airless packaging and compatibility testing with primary packaging.
- Reliable communication, development follow-up and willingness to build a long-term collaboration.
Manufacturing quality and certifications
- ISO 22716 / GMP cosmetic manufacturing standard.
- Clear quality control process for raw materials, bulk and finished product.
- Batch traceability and production records.
- Preferably experience exporting to or working for the European cosmetic market.
- Ability to provide standard factory certifications and compliance documents when requested.
Product and pack compatibility expectations
- Support for airless pack selection aligned with a minimal clinic positioning.
- Compatibility testing between formula and packaging.
- Guidance on fill volume, pack sourcing and practical MOQ constraints.
- Ability to provide or coordinate artwork technical specs, labeling zones and pack documentation.
Documents and technical information expected for the formula
- Complete INCI list and quantitative formula information when possible under the agreed framework.
- Raw material documentation for the formula components, including technical data and safety support files where applicable.
- COA for production batches.
- SDS / MSDS where applicable for raw materials or required technical documentation.
- Specification sheets for bulk and finished product.
- Microbiological, stability and compatibility test information available for the formula or sample stage.
Help needed for EU launch documentation
We are particularly interested in manufacturers that can either provide the necessary base documentation directly, or actively help coordinate it with the relevant partners so that the product can be placed on the European market correctly.
- Support with documentation needed for PIF preparation.
- Support or guidance for CPSR / safety assessment.
- Support for data required for CPNP notification.
- Assistance providing formula, raw material and packaging documentation needed by the safety assessor.
- Clarification on which parts are handled by the factory and which must be handled externally in Europe.
Main points to clarify with each manufacturer
- Can you manufacture a 4% niacinamide barrier serum for sensitive skin?
- What is your MOQ for bulk and for finished packaged units?
- Can you work with custom formulas or adapt a concept formula?
- Can you provide the documents needed for PIF, CPSR and CPNP support?
- Which tests are included: stability, microbiology, compatibility, preservative challenge?
- Can you support airless packaging and formula-pack compatibility?
- What is your sample process, lead time, production lead time and payment structure?
- Do you already work with brands selling in the EU market?
Small first launch with long-term vision
The objective is to start with a serious but realistic first production, supported by correct documentation and a technically credible formula, then build a long-term relationship with a manufacturer able to grow with the brand.