Quality, Testing & PIF
Documentation and quality processes appropriate to the project.
From manufacturing records to product documentation.
Expand each topic to explore quality and documentation needs.
Quality Management
Process and batch records are managed according to product requirements.
The applicable scope and documents must be agreed per project.Stability & Compatibility
Plan testing suitable for the formulation and packaging.
The applicable scope and documents must be agreed per project.Ingredient & Formula Data
Support INCI and other formulation-related documentation.
The applicable scope and documents must be agreed per project.PIF Document Support
Supply relevant documents; legal responsibilities remain with the appropriate responsible party.
The applicable scope and documents must be agreed per project.SA Sign-off
Help compile the information needed for safety assessment and arrange review and sign-off by a qualified Safety Assessor (SA).
Required documents, sign-off arrangements and scope are agreed for each product and project.Clear responsibilities improve project clarity.
Different products and markets may require different testing, authorizations and documentation.
Lead times, minimum order quantities, design responsibilities and verification plans are agreed project by project.