Acompliance-first, end-to-end partner
Beyond handing over a blend or a static concept, we guide a gated,evidence-based path: brief → pilot → post-launch refinement, with measurable checkpoints and full documentation packs. Expect clear boundaries, defined success metrics, and a focus on what truly scales.
We combine platform thinking with evidence-based iteration. Rather than a one-off concept,we co-design a path that balances oxidative robustness, sensorial targets, and regulatory readiness from day one.
Identify. Comprehensive ingredient selection and constraints mapping (ISO 16128, REACH status and success metrics), establishing a solid reference baseline for the project.
Design. Selection of the base edition and definition of the HLB route, pH window, rheology target and sensorial profile of the formula.
Evaluate. Accelerated stability testing (40 °C / RT / 5 °C), freeze–thaw cycles, centrifugation, d90 and pH drift, with ISO 11930 planning or execution when required.
Adjust. Optimisation of the emulsion and lipid phase, confirmation of packaging–formulation compatibility and preparation for pilot transfer (CPPS / CTQ).
A streamlined flow unifying creation, adaptation, and evolution. Our process starts with Intake & Criteria, where we frame constraints, markets, claims and risk appetite, and continues with Ingredient & Route Mapping, selecting viable lipid routes, preservation strategies and regulatory-safe options. In Platform Design, we define the Edition base and the technical framework of the formula before moving into Prototype Sprint where the first variants are built and challenged under demanding conditions.From there, Evidence Pack & Compliance consolidates data and ensures the formula is ready for scrutiny and registration, while Scale-up Readiness translates the concept into industrial parameters. When required, Adaptation & Localization fine-tunes the project to regional regulation, cost structures and market nuances, and Evolution & Discovery keeps a continuous improvement loop open post-launch, integrating feedback, new actives and greener routes into future Edition cycles.
Reference deliverabless (under NDA and project scope): platform spec, batch sheets,stability charts, ISO 16128 report, ISO 11930 plan/result, transfer dossier.
Every strong formula begins with dialogue. Share your brief and constraints, and we’ll help you identify the right ESSENTIKA — SQA starting point, documentation pathway, and transfer plan, so you can move faster with fewer reformulation loops.