Benefits
Planning certainty over problem-solving
Decision-making instead of coordination
Early sample availability enables decisions based on real products.
This reduces coordination loops and relieves product management.
Faster from trend to scalable production
Targeted adjustments instead of full redevelopment speed up development, reduce costs, and accelerate production readiness.nt times, lower costs, and accelerate the transition to production.
Products
Labtree evaluates cosmetic trends for feasibility and makes them available as early samples.
Brands can assess, adapt, and decide based on real products before committing resources.
100% clean formulations
Services
From idea to reliable launch
Labtree structures cosmetic development into a clear process with defined timelines, transparent costs, and clear responsibilities.
This keeps projects controllable without adding coordination overhead.
White Label
Market-ready and tested formulations that can be specifically adapted. For quick market entries with low development effort.
Private Label
New developments based on individual requirements. For brands that want to differentiate themselves without building operational complexity.
Design
Product and packaging design for clear positioning and consistent brand impact. Newly developed or implemented according to specifications.
Packaging
Suitable primary and secondary packaging tailored to formulation, functionality, and brand positioning. Technically compatible and safe.
Regulatory
Analytics, studies, and regulatory documentation as part of the process. This creates legal certainty parallel to development.
Production
Manufacturing, filling, and packaging with a focus on quality and flexibility. For reliable delivery capability from the first batch to reproduction.
Frequently asked questions
When is a product market-ready?
The time frame until market readiness varies depending on the development approach. White-label products with standard packaging are typically deliverable within 2 to 3 months. Custom developments usually require 3 to 6 months due to stability testing and regulatory deadlines. Key time factors include the availability of raw materials and packaging as well as the completion of stability tests.
How is the sampling done?
Physical samples of prequalified formulations are shipped from the sample storage within 24 hours. For customers, the shipping of standard samples is free of charge.
What is the minimum order quantity (MOQ)?
The minimum order quantity is set to 1,000 pieces per product by default. The exact specification is determined during the project setup and is dependent on the target sales price, the chosen packaging, and the complexity of the production process. The aim of this quantity specification is to ensure economically sustainable production with marketable unit costs.
What is the difference to a classic contract manufacturer?
Classical contract manufacturers are primarily specialized in the utilization and operation of their own production facilities. In contrast, Labtree acts as a strategic orchestrator, taking over the technical, economic, and regulatory pre-qualification even before capital is tied up in production. Project management is centrally controlled through a digital partner portal, while production is realized through a qualified and flexible production network.
Who owns the rights to the recipe?
The ownership rights are individually regulated by contract. In the case of customer-specific new developments, the ownership rights (Intellectual Property) or exclusive rights can be transferred to the client. White-label standard formulations remain the property of Labtree and will not be disclosed.
How is planning security ensured?
Production capacities, raw material stocks, and availability of packaging materials are already evaluated in the conceptual phase. The Labtree Partner Portal serves as a central instance where all project steps, milestones, and regulatory documents (e.g., PIF, safety reports) are deposited. This enables real-time monitoring of critical paths and securing launch dates.
When is a white label solution appropriate and when is a new development worthwhile?
A white-label approach is recommended for a quick market entry with low development risk based on already tested formulations. A new development is necessary when specific active ingredient concepts, exclusive performance promises, or a technological differentiation are to be achieved in the market. The choice is made based on an analysis of budget, target market, and the required time-to-market.
How does the project kickoff proceed?
The process begins with an initial conversation to assess feasibility and to align budget and timeline. After project approval, access to the partner portal is activated. Through this interface, all subsequent phases – from sampling to regulatory approvals to final production and logistics – are managed and documented.
