Tablets (immediate-release, enteric-coated, controlled-release, bilayer, and orally disintegrating), capsules, oral liquids (bulk and final packaging), powders (bulk, bottles, and sachets), and buccal formulations are supported. If a specific dosage form is needed, contact us to confirm feasibility.

Yes. As per cGMP requirements, all raw materials undergo identification and heavy metals testing before manufacturing. Potency (assay) testing is performed on active ingredients for both raw materials and finished products. Our analytical lab is cGMP-certified, staffed by PhD scientists, and all testing data is reviewed and approved by an independent QA department. Clients can also provide their own Certificate of Analysis from a certified third-party lab.

Yes. Vici was founded by pharmaceutical scientists and specialises in formulation development, analytical testing, and small batch manufacturing. The team develops custom supplement formulations with quality built into every step — from ingredient selection through to final product testing.

Pilot launch batches are offered for qualified projects, with a clear path to commercial scale. Commercial minimums apply for ongoing production. Provide format and target volume for confirmation.

Yes. Established international contacts exist for sourcing high-quality, regulatory-compliant raw materials. Incoming ingredients can be tested in-house to certify and confirm all raw materials meet quality standards before manufacturing begins.

Product format, target order quantity, timeline, current stage (formula ready vs needs development), and any packaging preferences. The more provided upfront, the faster a clear path forward can be given.

No. Work spans founders at the early stage through established brands scaling commercial supply. What matters is seriousness about quality and a clear product in mind.