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To ensure you meet USP regulations regarding testing containers, AMRI provides testing for various classes of pharmaceutical glass.

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To qualify your plastic container for use with pharmaceutical-based products, AMRI provids specialized testing procedures based upon the specific type of plastic that the container is made from.

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AMRI provides testing for auxiliary packaging components in accordance with all requirements and revisions to current USP chapters.

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AMRI's experts provide a range of services that assess the container performance of your solid and liquid dose products.

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AMRI provides container qualification testing in accordance with European Pharmacopoeia (EP) and Japanese Pharmacopoeia (JP) regulations.

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AMRI conducts testing on elastomeric closures to determine the sterility of sterile product packaging.

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AMRI provides testing to determine the biological reactivity in vitro and in vivo of your plastic container components.

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AMRI offers comprehensive routine Pharmacopoeial container qualification testing

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R.D. Laboratories maintains a large array of analytical instrumentation capable of performing a wide variety of procedures.

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Shijiazhuang Rainbowlabs pharmaceutical Technology Co. Ltd (Rainbowlabs) is a FDA-inspected laboratory set up to provide high quality laboratory testing and services to pharmaceutical companies throughout the world.

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Our success as a leading service provider derives from the importance we attach to meeting and exceeding our customers’ expectations, while delivering quality products, on time, at a competitive cost.

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Characterization studies for your product can be conducted prior to formulation. We specialize in the design and execution of pertinent pre-formulation activities required for successful pharmaceutical product development.

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Based on more than 30 years of experience and application with an extensive range and type of products, our customers gain more knowledge, Innovation and technological expertise through the following services: Packaging screening for up-front stability.

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GVK BIO performs stability analysis of drug products and active ingredient (APIs), packaging as per ICH, quality control testing and release as per cGMP requirements.