01
Pharma DNA, not nutraceutical roots
20+ years making regulated APIs for the world’s strictest markets. 43+ US-DMFs. USFDA / EU-GMP / PMDA inspected. Our floor was already pharma when we started making nutra.
The same hands
that make Pharma,
now make Nutra.
20+ years of regulated-pharma discipline — 43 US-DMFs, 25 CEPs, four GMP sites inspected by the USFDA, EU authorities, PMDA and KFDA — now applied to our nutraceutical portfolio.
Our Nutraceuticals Portfolio
The Nutra Portfolio,
2026.
Vegan D3, Algal DHA, and Vitamin D2 are developed. Hyaluronic Acid, Glutathione, and Vitamin A are in the pipeline. Built on pharma standards, designed for nutrition.
Developed01 — 02
Also Developed03
In the Pipeline04 — 06
Why Symbiotec
Pharma rigor is the quiet difference.
01
Pharma DNA, not nutraceutical roots
20+ years making regulated APIs for the world’s strictest markets. 43+ US-DMFs. USFDA / EU-GMP / PMDA inspected. Our floor was already pharma when we started making nutra.
01 / 04
Why Symbiotec
Pharma rigor is the quiet difference.
Most nutraceutical makers work up from food-grade. We work down from regulated-API standards. Everything we ship is built on that inversion.
02
Biology replaces chemistry
Phytosterols through a 3-stage bioprocess. Schizochytrium fermentation with zero hexane. Fewer synthetic steps means fewer impurities — by design, not by retrofit.
03
Tested to ICH, not to food minimums
Heavy metals, microbials, residual solvents measured against ICH Q3D and pharmacopoeia limits. Same QMS, same batch records, same impurity profiling as our APIs.
04
One pharmacopoeia across every form
Crystal, oil, powder, spray-dried, custom premix. Ph.Eur. monograph 0072 / 0574 / 0575. One supplier, every format — without switching grades.
By the Numbers
Proof, not promise.
Our nutraceutical portfolio sits on the same regulatory and operational footprint that has served the world's most demanding pharmaceutical markets for 20+ years. Every number below is on file with a regulator.
US-DMFs
Filed across the world’s most regulated pharmaceutical markets.
CEPs
Certificates of Suitability issued by EDQM for European compliance.
KL fermentation
Aggregate live capacity — 400 KL of which is dedicated nutra.
GMP sites
USFDA · EU-GMP · PMDA · KFDA inspected, year after year.
Our Journey20+ years of
20+ years of
regulated craft.
From a single steroid API plant in 2002 to a dedicated nutraceutical hub in 2026 — each step inspected, each facility qualified.
Looking for a trusted plant-origin partner?
Tell us your market, application, and volumes. Our Nutra team replies within 1 business day.