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AMRI's experts provide a complete range of synthesis capabilities for sterile API projects, from raw materials through regulated early- and late-stage intermediates to bulk APIs.

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Biophore, is engaged in the development & manufacture of niche pharmaceutical products & modified oral solid dosage forms, Injectable / parenterals etc. It has emerged as a trusted partner in the generic industry across US, EU & other regulated markets.

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In our mission to be a leading manufacturer in the pharmaceutical industry we have built a state-of-the-art facility which is as per US FDA & EU GMP standards. We have capabilities for manufacturing Oncology APIs, General & Bulk Sterile APIs.

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PrJSC Indar manufacturing plants worldwide managed to implement full technological cycle of insulin production – from fermentation to finished dosage forms. The only in Ukraine manufacturer of animal origin insulin (porcine)

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We perform sterilization (method according to European Pharmacopoeia) to produce active ingredients and excipients free of germs capable of reproduction (sterile). This can be followed by further production steps such as micronisation, blending and packin

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The business approach of Fresenius Kabi Product Partnering is to provide our customers integral support throughout the life-cycle of their parenteral products: Starting at the early stages through to full commercial scale, covering development as well as

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AbbVie contract manufacturing's additional commercial services capabilities include batch & continuous sterilization.

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Dalton offers the manufacturing of sterile cGMP APIs by a variety of methods including sterile filtration and dry heat sterilization. Our sterile product manufacturing capabilities include sterile filling of powders, liquids and lyophilization.

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Pfanstiehl can create custom solutions to address your unique high purity, cGMP component requirements.