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IN India
Stand No: 91A61
ACME is a leading manufacturer of Tablets, Capsules, Injectables, Oral Contraceptives & Levothyroxine Tabs. Our sites are approved by EU GMP, UK-MHRA, PICS, INVIMA, ANVISA, FDA Philippines, DAV Vietnam Ethiopia, Tanzania, WHO Geneva. Triggered: TGA Australia, Health Canada and US FDA by filing planned in Q1 2018. Offerings: CTD Dossiers for Licensing Contract Manufacturing Services Contract Development& Research Approvals: Asia: Nepal, Sri Lanka, Philippines, Vietnam, Cambodia, Laos, Thailand, Yemen, Myanmar Africa: Ethiopia, Nigeria, Ghana, Tanzania, Kenya, Uganda, Zambia, Malawi, Nigeria, Sierra Leone, Madagascar, Angola, Zimbabwe, Mozambique, Cameroon, Senegal, South Sudan North America: US & Canada (Filing planned in Q1 2018) Europe: United Kingdom, Hungary South America: Brazil, Colombia, Guatemala, Nicaragua, Paraguay, Uruguay, Chile, Costa Rica, Venezuela, Peru CIS: Kazakhstan, Uzbekistan, Ukraine ANZ: Australia Responsibility of product patents lies with the buyer of the country For more details please visit our website: www.acmeformulation.com& www.immacule.in
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Bilfinger Industrietechnik Salzburg provides turn-key biotech equipment, clean media preparation systems, piping and maintenance for the whole plant life cycle. It has its own locations in Germany, Austria and Switzerland as well as regional operations in China, South Korea and Eastern Europe.
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GB United Kingdom
Stand No: 40G42
ChargePoint Technology are market leaders in powder containment and aseptic transfer valves providing operator safety and sterility assurance for the pharmaceutical, biotech, chemical and other process industries.
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Sub-event: PMEC
Zone: PMEC
IT Italy
Stand No: 40J50
Comecer is a confirmed leader in isolation technology for pharmaceutical, chemical, and food industry applications. Its product portfolio covers various standard applications, but also high-quality customised solutions thanks to specific expertise acquired over the years. Continuous technological updating and the specific client requirements contribute to ensure operator safety and product sterility. For containment: isolators to handle highly active principles or excipients (ATEX, where required), isolators to load reactors, multi-stage isolators for chemical synthesis or laboratory operations. For asepsis: isolators for sterility tests and formulation of sterile drugs, isolators or RABs integrated into the liquid or powder filling lines. Solutions aimed at Grade A pharmaceutical continuity is then added: RABs, laminar flow trolleys, transfer hatch (with peroxide sterilisation, where required). Comecer's objective is to respect the fundamental safety and quality requirements, not only internally but especially towards the end client.
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Sub-event: PMEC
Zone: PMEC
FR France
Stand No: 40H40
Getinge's portfolio of GMP washers, sterilizers, closure processing systems, isolation technology and sterile transfer systems, provides solutions for our customers' unique challenges and strict compliance requirements while achieving high performance, maximum productivity and streamlined processes. Isolators: both soft wall and rigid wall, for sterility testing, toxic drug preparation, etc. The Moduline™ compact isolated filling line and the Moduline Biodecontamination™ using nitrogen dioxide for treatment of tubs containing syringes or vials, on aseptic isolated filling lines. DPTE® transfer ports for immediate secure connections. Sterile packaging: ready-to-sterilize and pre-sterilized DPTE BetaBag® products for a variety of applications, assembled in our state-of-the-art clean rooms.
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Sub-event: PMEC
Zone: PMEC
IT Italy
Stand No: 42C20
Haemopharm is a pioneer company in the manufacturing and commercialization of flexible bags for sterile solutions and for dialysis. A widely consolidated know-how and continuous research enables Haemopharm to produce different types of flexible bags and medical devices for pharmaceuticals applications: from standard size bags, made to contain infusion and dialysis solutions, to bags especially made for nutrition, washing, blood and tissue preservation, pharmaceuticals gels and powders, antibiotics as well as bags suitable for cryopreservation and inert to gas for ozonetherapy. Haemopharm used in production materials like PVC, PP (multy-layer), EVA, PVC DEHP-free. Haemopharm has a few branded products and CE marked products, used for instillation, washing, pharmacy compounding and others. Haemopharm is certified by UNI EN ISO 9001:2008 and UNI EN ISO 13485:2007.
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Sub-event: InnoPack
Zone: InnoPack
IN India
Stand No: 60B11
Piramal Pharma Solutions is a Contract Development and Manufacturing Organization (CDMO), offering end-to-end services required to bring a drug to the market place faster. We offer Pharmaceutical Development and Manufacturing solutions through collaborative partnership models and we work with our customers throughout the drug life cycle.
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Sub-event: CPHI
TR Turkey
Stand No: 91A43
New
Founded in 1986 in Istanbul, Polifarma Pharmaceuticals is focusing its product range on several packaging alternatives in LVP, including the production of vials and ampoules in SVP. Polifarma's modern parenteral solution production facility uses advanced technology equipment and operates in compliance with the norms of current Good Manufacturing Practices (c-GMP), and is capable of manufacturing products in the form of glass / PVC and PP, simultaneously.
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DE Germany
Stand No: 40D20
Rommelag ENGINERING is the inventor and worldwide leader of the Blow-Fill-Seal technology (BFS): bottelpack® aseptic-filling machines for packaging of sterile liquids, creams and ointments. The bottelpack machines are designed to blow, fill and seal during the same manufacturing process, which gives the guarantee to keep the sterility of the products. The machine capacities reach up to 30,000 containers per hour depending on container sizes which vary from 0.1 ml to more than 1,000 ml. Plastic materials used are PE, PP and others. For customer-specific container and closure developments as well as for test and contract fillings own laboratory test and production utilities are available. Rommelag ENGINEERING also manufactures leak detectors, cap welding machines and inspection systems which can be integrated inline into the packaging system.
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GB United Kingdom
Stand No: 61D32
Symbiosis is a contract pharmaceutical manufacturing organisation (CMO) that specialises in the GMP manufacture and sterile fill/finish of vials of drug product for clinical trials and low-volume commercial supply. The core strengths of the company include regulatory compliance, technical capability and operational flexibility. Specialist manufacture of injectables takes place in a purpose-built MHRA-licensed facility, enabling Symbiosis to handle products that require aseptic liquid filling or lyophilisation for a range of complex biologic or small molecule drugs. Offering fast access manufacturing slots and accelerated release of drug product, Symbiosis is ideally primed to service demand for small-scale, fast-turnaround while providing drug product manufacturing excellence and ensures regulatory compliance to the highest standards.
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Sub-event: CPHI
CA Canada
Stand No: 40G64
Vanrx Pharmasystems makes the most technologically advanced aseptic filling solutions for the pharmaceutical industry. Vanrx pharmaceutical filling machines use robotics, machine vision and gloveless isolator technologies to automate the packaging of injectable drugs into vials, syringes and cartridges. The company was founded by pharmaceutical industry veterans to create the systems needed to make the next generation of innovative therapies. For more information, visit www.vanrx.com.
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Sub-event: PMEC
Zone: PMEC
DE Germany
Stand No: 41K70
Vetter is a leading contract development and manufacturing organization (CDMO) that specializes in the aseptic filling of syringes, cartridges and vials. The company has extensive experience with biologics and other complex compounds, including monoclonal antibodies, peptides, interferons and vaccines. Collaborating with pharma/biotech clients worldwide, Vetter supports products from preclinical development through global market supply. Through its U.S. and European facilities, Vetter Development Service provides state-of-the-art support for early-stage products, with seamless transfer at Phase III to Vetter Commercial Manufacturing for large-scale production. The company offers state-of-the-art technology and innovative processes to promote product quality and maximize API yield.
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