A standard you can read.
Exact doses, third-party testing on every batch, and a 50-person beta before launch. The standard evolve® is held to, in full.
01 · The system
Most supplement advice ignores the clock.
Cortisol peaks shortly after waking. Adenosine builds through the afternoon. Recovery does its heaviest work at night. One formula, taken at one moment, cannot serve all three.
evolve® is designed backwards from that cycle. Rise carries the morning. Dream carries the night, melatonin-free and non-habit forming. Base runs daily underneath both.
02 · The effects
Morning output. Daily foundation. Night recovery.
Hours after Rise
03 · The formulas
Clinically dosed. Fully disclosed.
No proprietary blends. Every ingredient appears on the label with its exact amount, and its standardisation where one applies.
The amounts are clinical-level: L-Glycine at 2150mg in Dream, creatine monohydrate at 5g in Base, mushroom extracts standardised to 40% polysaccharides.
[2] Kreider RB et al. International Society of Sports Nutrition position stand: safety and efficacy of creatine supplementation in exercise, sport, and medicine. JISSN, 2017.
[3] Bannai M, Kawai N. New therapeutic strategy for amino acid medicine: glycine improves the quality of sleep. Journal of Pharmacological Sciences, 2012.
04 · The beta
Tested while it could still change.
The beta ran while formulation was still open. What came back moved the final doses, ratios and formats. Designed to change the formulas, not to produce marketing numbers.
[1] EV-01. evolve® formulation beta, N=50. Rise and Dream taken daily for 14 days, 2026. Participant feedback informed the final formulas. Focus and sleep figures are self-rated changes against enrolment baseline on a 10-point scale; improvement was self-reported.
05 · The testing
Every batch, not a spot check.
'Third-party tested' appears on almost every label. It rarely says which tests, how often, or against whose limits.
evolve® specifies. Each batch is tested by laboratories with no stake in the result, against limits written into EU law.
Batch testing
Independent laboratories test every batch for identity, potency, heavy metals, microbiological contamination and pesticide residues, against EU food-safety limits. Allergen testing covers all 14 allergen classes listed in Annex II of Regulation (EU) 1169/2011. No skip-lot testing, and the Certificate of Analysis is available on request.
Manufacturing and hygiene
Made in the Netherlands under cGMP, with HACCP food-safety controls to Regulation (EC) No 852/2004. Packaging meets EU food-contact standards, including the migration limits of Regulation (EC) No 1935/2004.
Traceability
Each batch carries a unique identifier, documented from raw material through production and distribution, in line with Regulation (EC) No 178/2002.
Labelling and claims
Every ingredient appears on the label with its exact amount, and vitamins and minerals are declared against EU reference intakes under Regulation (EU) No 1169/2011. Only claims authorised under Regulation (EC) No 1924/2006 are used. Where an ingredient has no authorised claim, it is listed by amount, not by promise.
[ founders ]
Read the label. Then decide.
Everything this page claims is printed on the panel. The founders list gets early access and the founding rate.
