Question 1

What does a natural medicine CRO like MedGence do?

Accepted Answer

MedGence provides end-to-end research and development for plant-derived ingredients: active ingredient screening, potency evaluation by origin and season, analytical method establishment, process studies, toxicity, in vitro, animal and clinical studies, natural formulation research and contract manufacturing of active ingredients and finished products.

Question 2

Can one partner take my botanical project from lab research to commercial supply?

Accepted Answer

Yes. Our own pilot plant and collaborative factories are directly managed by our technical team, so validated study results transfer smoothly into OEM/CDMO production of extracts and finished dosage forms.

Question 3

Which analytical techniques are used to establish quality standards?

Accepted Answer

Depending on the product, methods include high-performance thin-layer chromatography (HPTLC) identification, high-performance liquid chromatography (HPLC), gas chromatography (GC) and chromatographic fingerprinting.

Question 4

How is my formula and process know-how protected?

Accepted Answer

We work on an entrusted contract research and manufacturing model under non-disclosure, so your product information, formulas and process parameters are not disclosed and your competitive advantage is preserved.

Question 5

Which dosage forms can MedGence develop and manufacture?

Accepted Answer

Active ingredients can be supplied as concentrated liquids, powders, pastes and volatile oils. Finished products include oral liquids, capsules, softgels, tablets, soluble powders and granules.

Question 6

Do you support clinical studies for new drug applications?

Accepted Answer

Yes. We arrange small-group human trials for dietary supplements as well as Phase I, II, III and IV clinical studies to help clients obtain the data required for a new drug application (NDA).

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