Contract manufacturing of dietary supplements

MiraxBioPharma offers contract manufacturing services for dietary supplements under private label (PL), in accordance with quality management system standards based on HACCP principles. The production of dietary supplements is carried out in cleanrooms that meet Class D cleanliness standards (as applied in pharmaceutical manufacturing).

We are ready to deliver a full turnkey solution

From formulation development to full-scale production, ensuring high-quality processes at every stage

We provide labeling for jars and boxes, as well as packaging of dietary supplements for online marketplaces

Dosage forms

Tablets, hard-filled capsules, liquid-filled capsules, sachets, vials, and bottles

Packaging options

Blisters, jars, boxes

We will help you create a high-quality, effective, safe, and in-demand product within a reasonable timeframe and without unnecessary costs

Contact us to discuss your project and receive a detailed consultation

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Filling out these documents will significantly speed up the processing of your request and the cost calculation

Download the documents and fill in the required information. If you have already submitted the form, you can send the documents and your request to our e-mail cp@mbpharma.ru including your contact details

Client's Terms of Reference for the Development and Commercial Production of Dietary Supplements

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Pharmacovigilance

MiraxBioPharma is committed to ensuring the quality and safety of its products and pays special attention to collecting and analyzing information about adverse reactions and complaints associated with the use of our products.

If you become aware of any adverse reactions to the medicinal product Cezarox® Epi or of a lack of therapeutic effect, please report it via email at: adversareaction@drugsafety.ru or by phone: +7 (800) 777-86-04.

If you become aware of any adverse reactions to other MiraxBioPharma medicinal products or of a lack of therapeutic effect, please report it via email at: GVP@mbpharma.ru, by phone: +7 (495) 721-50-58 or by filling out the electronic form below

Adverse reaction reporting form
Specify gender*
Suspected medicinal product information
Reporter information

Preferred method of contact*
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