Formulation Assessment
Assessment of the formulation in relation to the intended application, product category and project-specific requirements.
Quality Assurance & Product Safety
PLCC integrates quality assurance and product safety into your private-label project from the outset — with coordinated testing, defined approvals and transparent processes from development to finished goods.
Safety from the outset
During product development, formulation, application, packaging and intended target market are already considered together. This allows relevant quality and safety requirements to be identified early and integrated meaningfully into further planning.
Which tests are necessary or recommended depends on the product type, formulation, packaging, intended shelf life and planned product claims. The testing scope is therefore defined for the specific project rather than applied as a standard package.
Our Quality Areas
The following areas work together and are planned individually depending on the product, packaging and project scope.
Assessment of the formulation in relation to the intended application, product category and project-specific requirements.
Suitable tests support the assessment of whether appearance, colour, odour and consistency remain stable over the intended period.
Formulation and primary packaging are assessed together so that packaging component, material, dosage and application work reliably as a system.
Depending on the formulation and product type, microbiological testing and other product-specific assessments can be integrated.
Defined control and approval steps accompany manufacturing, filling and secondary packaging through to finished goods.
Relevant project data, test results and approvals are recorded in a structured manner and brought together transparently.
Quality and Market Readiness
Quality tests show whether the product and packaging function reliably in the intended use. Regulatory Affairs translates the relevant results and product information into the requirements of the respective target market.
Quality Assurance
Regulatory Affairs
For products intended for the European market, the relevant requirements of the EU Cosmetics Regulation and Good Manufacturing Practice are considered within the project.
Explore Regulatory AffairsCustom Testing Strategy
A water-based serum has different requirements from an anhydrous balm, mascara or body-care product. Packaging, shelf life, application and intended product claims also influence the testing strategy.
Water content, ingredient system and product properties determine which tests are appropriate.
Skincare, decorative cosmetics and special application formats bring different quality requirements.
Material, dispensing system, light protection and contact surfaces need to suit the product and intended use.
Market, labelling, claims and specific requirements are included in the planning at an early stage.
The Quality Process
Quality assurance is planned throughout the project and coordinated with development, packaging, regulatory and production.
Product type, application, target market, packaging and special requirements are defined together.
The selected or developed formulation is assessed in the context of the planned product and its use.
The required testing scope is defined, carried out and evaluated specifically for the project.
Defined controls accompany manufacturing, filling, secondary packaging and final product approval.
Relevant test results, decisions and approvals are brought together in a structured and transparent manner.
Your Benefits
Quality and safety requirements are considered during the development phase.
Defined testing and approval steps create transparency throughout the project.
The testing scope is aligned with the formulation, packaging, product type and target market.
Structured controls support consistent product characteristics and reproducible results.
Connected Throughout the Project
Good quality is not created in an isolated step. It connects development, formulation, packaging, regulatory, manufacturing and project management.
Integrate quality requirements into the product concept from the outset.
Learn more → 02Select the formulation, sensory profile and application to suit the project.
Learn more → 03Align formulation, packaging component, dosage and application.
Learn more → 04Defined controls throughout production and secondary packaging.
Learn more → 05Prepare product information and market readiness from a regulatory perspective.
Learn more → 06Coordinate testing, approvals and the project areas involved.
Learn more →Frequently Asked Questions
You can find further general information about development, packaging, production timelines and regulatory requirements in our central FAQ.
View all FAQsThe specific testing scope depends on the formulation, product type, application, packaging, target market and desired product claims. It is therefore defined individually for each project.
Ideally during product development. This allows the formulation, packaging, testing requirements and target market to be aligned at an early stage.
The primary packaging is in direct contact with the product and influences protection, dosage, application and stability. Formulation and packaging therefore need to be considered as one system.
Quality assurance evaluates and controls the product, packaging and process. Regulatory Affairs coordinates product-related information and formal requirements for the intended target market.
Yes. Relevant project data, test results, decisions and approvals are recorded in a structured manner and brought together transparently throughout the project.
Your Private-Label Project
Tell us about your product idea, target market and requirements. Together, we will plan the appropriate quality, safety and approval steps.
Send a non-binding project enquiry