Project-appropriate controls
Applicable control points are defined according to the product and its development stages.
Quality & commitments
Trust is built on verifiable information.
This page describes only general practices that can be presented without attributing an undocumented label or approval to the laboratory.
Quality & commitments
Clear commitments, from brief to finished product.
Each project is framed according to its nature, maturity and the supporting information that is genuinely available.
Document traceability
Useful project references and documents are organized to keep an understandable record of approved choices.
Documented commitments
References to standards, labels or approvals will be added only after supporting documents have been received and checked.
This content will be completed when supporting documents are available.A control journey defined for each project.
These stages structure quality vigilance without replacing the control plan specific to each product.
Raw material selection
Useful references, characteristics and documents are identified according to the formula and target market.
Formulation & R&D
Monitoring criteria are clarified during development without turning the brief into an undocumented promise.
Production monitoring
The elements required for manufacturing are approved before production is organized.
Appropriate controls
The control plan is defined for the product. Microbiological or physicochemical controls are mentioned only when applicable and documented.
Packaging control
The container, format and information to display are checked against the choices approved for the project.
Final verification
Project references and documents are reviewed for consistency before final approval.
Tell us about your project.
Describe your needs at your own pace. Open choices can be defined with the GB2 team.