Bionetic
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Bionetic
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Bionetic
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Behind every capsule
Every Bionetic formulation is produced in GMP-certified European facilities under pharmaceutical-grade quality controls. We test everything. Twice.
All manufacturing happens in facilities certified to EU GMP and ISO 9001 standards — the same baseline pharmaceutical manufacturers must meet.
Every active ingredient is sourced from a single audited supplier with full chain-of-custody documentation. No middlemen, no commodity blending.
Each batch is independently tested for identity, potency, heavy metals, microbial contamination, and residual solvents by an accredited third-party laboratory.
Certificates of analysis (COAs) are available on request for every batch. We publish standardisation specs on every product page.
Our process
Identity confirmed by HPTLC and FTIR. Heavy metals quantified by ICP-MS. Microbial limits validated before any ingredient enters production.
Weight, blend uniformity, dissolution, and active content measured at multiple checkpoints during encapsulation and packaging.
Final assay against label claim. Stability testing for shelf-life confirmation. Independent third-party verification before release to market.
Certifications & standards
Researchers and partners can request batch-specific COAs directly from our scientific team.
Contact our science team