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Minakem provides fully integrated and technology-oriented contract manufacturing services ranging from process development, kilo lab & pilot scale-up through to full industrial scale manufacturing of complex molecules including HPAPI’s.

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With the best in class manufacturing facilities and state-of-the-art research platform besides our R&D we have embarked on establishing contract manufacturing organization for APIs, Advanced Intermediates & Intermediate for Controlled Substances.

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Medichem offers a wide range of contract services, may that be manufacturing of APIs (including HPAPIs) or manufacturing and packaging of the finished dosage form, testing and release services.

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Polpharma is the largest Polish manufacturer of APIs and world leader in the manufacture of hydrobisphosphonates. Total capacity of our reactors for substance synthesis is 350,000 litres.

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Phyton Biotech offers clients a full range of integrated contract product and process development and commercial manufacturing services across the entire development chain, from feasibility to commercial production.

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All custom synthesis and contract manufacturing projects are governed by a flexible and effective management system with the aim of optimising the time to market, while maintaining the highest quality standards and minimising development costs.

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LEBSA is able to offer contract manufacturing services from grams to tones in accordance with GMP requirements.

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Malladi is a leader in manufacturing Ephedrine & Pseudoephedrine salts. We provide contract manufacturing services for a wide range of APIs & intermediates. Our GMP compliant manufacturing facilities are state-of-the- art facilities approved by USFDA.

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Temad Co. leverages its bulk production capacities created in past several years, to offer contract manufacturing services, in scales of 1 to 1000 kg, to API manufacturing

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Biophore, is engaged in the development & contract manufacture of niche pharmaceutical APIs, 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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ScinoPharm offers a wide array of process R&D services & API manufacturing capabilities designed to satisfy customers' exact requirements & facilitate their rapid market introductions. ScinoPharm specializes in process R&D & the production of cGMP APIs.

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In addition to contract manufacturing, Orofino Pharmaceuticals Group can offer a range of qualified services particularly in the quality, technical and regulatory areas.

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Drug’On Pharma Switzerland was the last company to be set up in the Orofino Pharmaceuticals Group. The Group bought out the ex Knoll and Abbott manufacturing site in Liestal,Switzerland. The chemical manufacturing site produces active pharmaceuticals ingredients (API) and intermediates.

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The Dishman CRAMS business offers an unparalleled range of facilities dedicated to contract manufacture of APIs, Highly Potent APIs (HPAPIs) and advanced intermediates & speciality chemicals for pharmaceutical customers.

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Zach Avrillé site has a long tradition in process development & API/ pharmaceutical intermediates manufacturing. About 215MT of APIs and GMP intermediates are manufactured each year.

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BioSpectra is a FDA registered, cGMP compliant, contract manufacturer and commercial producer of biological buffers, pharmaceutical excipients and laboratory reagents.

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Your GMP “One-Stop-Shop”, Angelini Fine Chemicals is a Contract Development and Manufacturing Organization (CDMO), which is fully dedicated to third party manufacturing of APIs, IMs and NCEs for the pharmaceutical and small molecule biotech industry.

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We manufacture and supply APIs through our sites in North America, Europe, and Asia. Our API facilities have been inspected and approved by several global regulatory bodies including the US FDA, Japan PMDA, UK MHRA and meet the cGMP compliance standards.

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Our API manufacturing plant specialises in the manufacture of cephalosporin active pharmaceutical ingredients (APIs). Our manufacturing complex has been successfully audited by leading global regulatory agencies like the US FDA, UK MHRA, GMP, EDQM, TGA , Danish Medicines Agency.

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Two of Avara’s sites provide contract development and manufacturing of active pharmaceutical ingredients (API). All facilities worldwide have a long-term record of quality and regulatory compliance.

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Neuland is a no-compromise, API manufacturing service provider, offering worldwide compliant manufacturing facilities to its customers that it guarantees not to compete with in finished product.

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Avra Laboratories is a Hyderabad based contract research & manufacturing services (CRAMS) company focused on: Providing high-end contract research and manufacturing services; Manufacturing of niche intermediates and APIs covering various therapeutic areas including oncology.

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Our ability to move quickly from the R&D laboratory to multi-kilo amounts into the pilot plant or into full production is a strength at Flamma. We have the flexibility to look at our sites to determine the best place to manufacture your materials.