TimeFlys works across botanical extracts, chemical synthesis, proven efficacy actives, fermentation-derived ingredients, foundational actives and custom active development.
Our technologies can support skincare, scalp care, hair care, body care and other personal care applications, depending on the ingredient and project scope.
Yes. We can build a customised development pathway around your target application, efficacy goals, formulation requirements and market positioning.
Yes. Early-stage support may include feasibility assessment, technology-route selection, raw-material screening and preliminary development planning.
We evaluate the desired benefit, ingredient type, formulation environment, target market, development timeline and evidence requirements.
Botanical extracts are plant-derived ingredient solutions developed through controlled extraction, enrichment and standardisation processes.
We focus on defined functional molecules that require controlled molecular identity, purity specifications and scalable production routes.
These are ingredients produced through controlled biological processes and may include peptides, polysaccharides, metabolites and postbiotic fractions.
Foundational actives are reliable ingredients used to support hydration, skin barrier care, texture, scalp care and general formulation performance.
Yes. Custom projects may combine botanical extraction, fermentation, synthesis and application testing when technically appropriate.
Yes. We can assess opportunities involving purity, stability, standardisation, process efficiency, compatibility or technical positioning.
Timelines depend on technical complexity, testing requirements and scale-up needs. A preliminary schedule is provided after feasibility review.
We collaborate with cosmetic brands, formulators, ingredient companies, research teams, manufacturers and international development partners.
Please provide the target application, desired benefit, preferred technology, formulation constraints, target market, expected volume and timeline.
Sample availability depends on the ingredient and project stage. Sampling conditions are confirmed after the technical requirements are reviewed.
We can provide compatibility guidance and application-oriented support within the agreed project scope.
Quality requirements are defined through specifications, analytical criteria, process controls and batch-consistency considerations appropriate to each project.
We can help design a fit-for-purpose testing strategy and coordinate suitable analytical, in-vitro, ex-vivo or instrumental evaluation through qualified partners.
We can help organise technical documentation and identify regulatory considerations, but final market compliance should be confirmed by qualified regulatory specialists.
Yes. Depending on the project, documentation may include specifications, technical data, development summaries and supporting evidence materials.
Confidential information can be handled under an appropriate non-disclosure agreement before detailed technical information is exchanged.
Intellectual-property ownership and usage rights are defined in the project agreement before development begins.
Minimum quantities depend on the ingredient, process, production partner and packaging requirements. They are confirmed during commercial evaluation.
Submit the R&D enquiry form with your project requirements. Our team will review the brief and recommend the most suitable next step.
