What else does Jarrow Industries offer?

Our facility offers superior manufacturing conditions for sensitive materials such as probiotics, effervescent formulas and highly hygroscopic materials such as SAMe. We have ultra-low humidity control, nitrogen flushing at various stages of processing, blister packaging including aluminum-aluminum and ACLAR and specialty coatings such as our proprietary natural, pH-sensitive enteric coating system.

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What measures does Jarrow Industries take to protect my intellectual property?

We will sign a non-disclosure agreement protecting our clients’ intellectual property.

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How can I be assured of the efficacy/ consistency of my products?

Our raw materials are rigorously tested to ensure that the quality, purity and potency meet or exceed requirements for dietary supplements as upheld by the FDA. We follow cGMP procedures and perform all analyses needed to ensure an accurate and safe
product. Science based formulations, state-of-the- art microbiology and analytical laboratories
ensure the efficacy and consistency of all the products we produce.

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What quality certifications does Jarrow Industries have?

We are cGMP Certified by NSF and Organic Certified by QAI. This means we are audited several times a year on our processes, documentations and almost all aspects of our manufacturing procedures.

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How long will it take to get my products?

Our average lead time is 10 weeks. However, it is possible for projects to be ready sooner or later as a variety of external factors can affect lead times. This includes availability of components, testing requirements, simplicity or complexity of the formulation and packaging design.

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Can you ship out of the country?

Yes, we can and will assist you with the necessary export documents.

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Can/will Jarrow Industries supply the raw materials for my product?

Yes, we source raw materials from the most respected and reputable suppliers in the industry including USP grade when this standard has been established. However, you may supply your own materials. Our guidelines require that every material is tested for conformity based on FDA Current Good Manufacturing Practices (cGMP) guidelines including vendor qualification per cGMP rules. We require a Certificate of Analysis (COA) and Material Safety Data Sheets (MSDS) on every material that enters our facility. If you provide your own material, your vendor must provide this documentation. We further use and determine testing standards as needed but begin with the information provided on the COA to ensure material identity, consistency and conformity.

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Does Jarrow Industries provide labels or supplement fact panels?

No, customers are responsible for providing their own artwork and labels. Once label art is prepared by the customer, the proof must be submitted to our Formulation and Quality Review teams to verify the accuracy of the supplement facts panel and compliance with federal regulations. However, we can refer you to excellent professionals to assist you in design as well as regulatory compliance.

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I already have a formula. Can Jarrow Industries manufacture it for me?

Yes, we can manufacture nearly any customer supplied formula which is considered a dietary supplement as defined by the United States Food & Drug Administration. Certain restrictions may apply.

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What are Jarrow Industries’ Research and Development (R&D) capabilities?

A team of highly skilled, qualified professionals can assist you with raw material sourcing andhelp formulate and manufacture a final product that will meet or exceed your criteria.

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