Quality built into every batch.
Defined specifications, applicable process controls, product-specific assessment, batch documentation and traceability from production to release.
Quality starts before commercial production begins.
Quality requirements aligned to product, process and market.
Every project has its own formulation, dosage format, packaging and destination-market requirements. We identify relevant quality considerations early and carry them through development, manufacturing, packing and batch release.
A defined quality path from brief to batch release.
The exact controls, testing requirements and documentation scope depend on the formulation, dosage format, manufacturing route and destination market.
Project review
Product purpose, dosage format, packaging, target market and documentation requirements are reviewed during the initial project assessment.
Material assessment
Relevant ingredient specifications, supplier documentation and material requirements are reviewed for the selected product.
Specification alignment
Relevant product parameters are aligned during formulation review, feasibility assessment and sample development.
Controlled manufacturing
Defined production parameters and applicable in-process checks support controlled, repeatable manufacturing.
Finished-product review
Product-specific parameters, applicable testing and relevant release documentation are assessed before commercial dispatch.
Batch traceability
Relevant production and quality records support traceability, accountability and future supply planning.
Testing aligned to the product and its requirements.
Identity & specification
Relevant identity or specification checks may be applied against defined material or product requirements, depending on ingredient and format.
Physical parameters
Applicable physical parameters may include appearance, weight, fill, dimensions or other product-specific characteristics.
Purity-related assessment
Relevant purity-related parameters may be evaluated according to formulation, raw-material risk, product category and destination-market requirements.
Microbiological assessment
Product-specific microbiological parameters may be assessed where applicable to the formulation, dosage format and product category.
Documentation that supports traceable commercial supply.
Documentation scope is assessed according to the product, manufacturing route, destination market and agreed commercial requirements.
Specific certificates, reports or documents should be confirmed before order finalisation. Availability may vary by product, facility and market.
Quality depends on clarity before, during and after production.
Align before production
Define the formulation, dosage format, packaging and relevant specifications before commercial production begins.
Control during manufacturing
Apply relevant production controls and in-process quality checks according to the selected manufacturing route.
Review before release
Assess relevant product, testing and documentation requirements before the batch is released for dispatch.
Quality and compliance must reflect the destination market.
A product suitable for one market may require different formulation, label, testing or documentation considerations in another. The intended destination market should therefore be identified at the start of the project.
Final regulatory responsibility, permitted claims and label approval must be assessed according to the regulations applicable in the destination market.
Ready to define the quality route for your product?
Share your product, dosage format, target market and expected order volume. Our team will review the brief and help identify the relevant quality, testing and documentation requirements.