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This means dividing the full reconstituted solution into smaller, single-use portions in separate sterile vials before the initial freeze

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Requirement & technical alignment 3-5 business days Decide: positioning, format, claim lane, regulatory pre-screen Exit: written roadmap + risk flags Sample development & lab optimization 7-14 business days Decide: prototype liposomal system, EE / sensory tuning Exit: evaluation-ready samples + open issues list Stability pre-testing 2-4 weeks Decide: accelerated stress, liposome integrity, oxidative retention Exit: pack / formula lock recommendation Pilot production & process validation 1-2 weeks Decide: cGMP pilot, parameter lock, reproducibility Exit: validated pilot release package Full-scale commercial production 2-4 weeks Decide: industrial run, full QC, packaging finalization Exit: market-ready batches + traceability pack Typical total: 6-10 weeks for standard programs

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