Exhibitors
International Medical Corps delivers lifesaving health care in emergencies for people affected by disaster, disease or conflict. No matter where, no matter what the conditions, they are the first there. They stay, long after the initial crisis ends, helping people survive and rebuild through the building blocks of recovery – water, food, safety, medicine. Their work is built on collaboration with local communities, transferring skills and knowledge to health care professionals and volunteers, even in the midst of an emergency response deployment. This helps lays the groundwork for faster, longer-lasting sustainable recovery.
INTEROR is a French 100% private company offering sophisticated intermediates (multi-steps synthesis and GMP). INTEROR employs 125 people, has a total capacity of 140 m3 made of half stainless-steel and half glass lined reactors ranging from 1 500 to 8 000 l and is specialized in high pressure hydrogenation, reductions, GRIGNARD reactions (large scale), bromination, chlorination, diazotation, SANDMEYER reactions, CLAISEN, DIECKMANN reactions. INTEROR's catalogue products are pyridines and piperidines, quinuclidines, chloroalkylamines, acid chlorides. Any product related to our product families can be developped. Any synthesis requiring above mentioned technologies can be studied with or without secrecy agreement.
Mexican company dedicated to manufacture active substances for the national and international markets, created in 1970 with the purpose of contributing with the development of the pharmaceutical industry. Leading manufacturer in the development and production of API.s. Constant compromise with investigation and innovation looking for a service of excellence.
Helping our
clients achieve Total Quality Assurance through custom, flexible, contract
services from a single source, our scientists, auditors and regulatory experts work with you at every stage of development, providing GMP and CMC Laboratory Services, GMP Auditing, GLP/GCP Bioanalysis, Regulatory and Toxicology Consulting and Pharmaceutical Manufacturing Support. Our Good Laboratory Practice (GLP) and Good Manufacturing Practice (cGMP) laboratory network have provided high quality technical services for some of the world's largest and most innovative pharmaceutical companies.
GMP and CMC Laboratory Services We provide regulatory-driven, phase-appropriate laboratory services in support of CMC programs seeing you through preformulation, formulation and product release. Our capabilities include centres of excellence for method development and validation, analysis, stability studies, extractables and leachables, solid state characterisation, cGMP quality control testing and cGMP batch release testing. Our teams have specialist expertise for complex medicines and drug delivery systems such as inhalation drug product development for pulmonary and nasal products or biologic therapeutics.
Pharmaceutical AuditingOur pharmaceutical auditing and management services give you a transparent view of your supply chain enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes. Through our shared audit programs, delivered by our global network of specialist auditors, you can benefit from rapid implementation, easier access to audit sites and potential cost savings.
Bioanalysis ServicesDuring preclinical and clinical development, our bioanalysis experts design and manage strategic work programs. Our expertise and industry insight aim to supply the answers you need as quickly and efficiently as possible. As a world leading provider of immunochemistry services and biomarker expertise for bioanalytical studies, we provide excellence in service delivery and support for your preclinical and clinical development of protein based therapeutics and other biologic medicines.
Regulatory and Toxicology ConsultingFrom discovery to commercialisation, our pharmaceutical regulatory consultants provide a fast-track and cost-effective approach to allow you to gain market access for products and assurance that they comply with global regulations.
Pharmaceutical AuditingOur pharmaceutical auditing and management services give you a transparent view of your supply chain enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes. Through our shared audit programs, delivered by our global network of specialist auditors, you can benefit from rapid implementation, easier access to audit sites and potential cost savings.
Intrograf Lublin is the leading manufacturer of printed folding cartons and leaflets for pharmaceutical sector with a production of over half a billion cartons and half a billion leaflets per year. Our products are distributed to over 90 different customers located both in Poland as well as in other European countries. We are committed to continuous improvement of our Production and Product Quality Control System in compliance with ISO 9001, ISO 15378 and GMP. Intrograf also operates in accordance with Editio Cantor requirements. We offer a variety of finishing processes which add a unique look, feel and functionality to materials. Thanks to our solutions your packaging attracts customer's attention and stands out from other brands. High-level expertise and a client-oriented approach is our hallmark. That is why we are able to fully understand your requirements and anticipate your needs. Choosing Intrograf means that you gain a reliable partner who will not only ensure the proper implementation of your orders but will also become your technological advisor.
With over 100 SKUs being supplied globally, Inventia is a rapidly growing FDF development and manufacturing pharmaceutical company, catering to over 80 partners. We offer end to end solutions from product development to supply of the finished product. Our highly skilled teams follow a QbD approach and utilize SAP systems to ensure the highest quality products reach our partners. We cater to over 30 countries from our Manufacturing facility based out of India, which has several regulatory approvals, USFDA, UKMHRA, KFDA, ANVISA, INVIMA, COFEPRIS, GMP SAUMP KFDA, FMHACA, Ghana FDA, JFDA, MCAZ, NAFDAC, PPB, TFDA, UAE MOH Uganda NDA.We believe in building and nurturing long-term relationships – with an aim to be the preferred development and manufacturing partner for any market.
Lipid excellence for the pharmaceutical industry - Made in Germany. IOI Oleo GmbH manufacturers its renowned lipid brands of hard fats and functionalized lipids for the pharmaceutical industry. Our production facility in Witten, Germany is US FDA-approved and GMP-certified. The most recent inspection by our German health authority took place in June 2018, which once again has confirmed our GMP-status. With decades of proven experience and excellence our lipid portfolio comprises of the following brands : MIGLYOL®, DYNASAN®, IMWITOR®, SOFTIGEN®, SOFTISAN® and WITEPSOL®
IOL CHEMICALS AND PHARMACEUTICALS LIMITED (IOLCP) is an existing profit making, listed Company (BSE Code 524164 and NSE Code: IOLCP). The Company is engaged in manufacturing of pharmaceutical APIs and industrial chemicals for use in various industries. In Active Pharmaceutical Ingredients, company has been producing - Ibuprofen, Metformin HCL, Clopidogrel Bisulphate II, Fenofibrate, Lamotrigine and UDCA. Products in API R&D pipeline are Pantoprazole Sodium, Gabapentin, Losartan Potassium, Domperidone, Fexofenadine, Pregabalin, Quetiapine Fumarate etc. In chemicals company has Ethyl acetate, Isobutyl Benzene (IBB), Monochloroacetic Acid (MCA), Acetyl Chloride etc. In Chemical R&D, company is coming up with Sorbitol 70% and Acetonitrile. For details please contact: Sunny Bali, International Business, Mobile :+91 9878996119, E-Mail: [email protected] and Ashwani Kumar, Domestic Business, Mobile : +91 9878996045, E-mail: [email protected]
IONISOS Group, is an international contract service company based in France and leads the French and Spanish sterilization markets. It specializes in radiation sterilization (gamma and e-beam) of pharmaceutical primary packaging, API's, finished pharmaceutical products & medical devices.
Hyundai Ki-Gong Co., Ltd. has designed and manufactured various automated industrial machinery, including semiconductor devices. In addition, Hyundai Ki-Gong Co., Ltd. has produced and developed. 10COLOR offset press, 7LAYER extruder, AUTOMATIC HEADING MACHINE, 5COLOR automatic silk printing machine, 4COLOR AUTO HOT STAMPING MACHINE, FOIL POLYMER TUBE MACHINE and all relevant molds, etc.
Hyundai Ki-Gong Co., Ltd. Application has registered over 80 patents related technologies, including intellectual property rights, etc. And Hyundai Ki-Gong Co., Ltd. and, iPACK Co., Ltd. has been merged and reorganized as iPACK Co.,Ltd. in order to make the organization based on high quality products and know-how accumulated and also in order to provide information, professional and focused in-depth knowledge. We are headed as a leader in the industry by operating quality management system based on the ISO. We have established operations subsidiaries and offices in Indonesia, including the United States and Japan and secured 15,000 square meters of floor space on 25,000 square meters of land for the annual tube production of 240 million. As a result, we are aiming to achieve exports of 5,000 million dollars
iPACK Co., Ltd. will provide the best value to customers for human pursuit of happiness, make up the foundation of self-realization to all employees including executives, and explore ways to develop cooperation with business partners.
Institute of Industrial Organic Chemistry Branch Pszczyna is a pre-clinical contract research organization specializing in toxicological and ecotoxicological studies. As a GLP (Good Laboratory Practice) certified Institute we provide a wide range of services in the fields of human health protection and environmental safety, conduct studies of: plant protection products, pharmaceutical products, veterinary medical products, food and feed additives, industrial chemicals, biocides and industrial wastes. IPO offers research services in compliance with international guidelines: OECD, EU, EPPO, EMA, US EPA, SETAC/IOBC/BART/EPPO and ISO.
Enterprise Ireland is the government organisation responsible for the development and growth of Irish enterprises in world markets. Our mission is to accelerate the development of world-class Irish companies to achieve strong positions in global markets resulting in sustainable economic growth. Enterprise Ireland works in partnership with Irish enterprises assisting them to start, grow, innovate and win export sales on global markets. Enterprise Ireland has a network of over 30 offices covering more than 60 markets worldwide, providing assistance to businesses in Ireland to connect with and maintain profitable partnerships with international companies.
i-Dositecno is a company dedicated to the developing and manufacturing of aseptic processing systems for pharmaceutical industry. We design and build sterile and aseptic filling machinery suited for oncology, biotechnology, biosimilars and ophthalmological products with a great variety of formats (vials, syringes, cartridges, eye-drops and Aptar devices). Fully servo-motorized machines, Scada software, according to the 21CFR Norm part 11, we comply the most demanding requirements in the industry. Proudly made in Barcelona.
As Istem Medikal employees, together with our business partners, we serve our customers by manufacturing and supplying innovative, reliable and environment friendly medical devices. We diligently value our brand and its benefit to society. Istem Medikal is an establishment that takes place in sales and marketing area of medical sector since 1995. In order to utilize its experience and accumulation which was gained by years , Istem Medikal founded its own manufacturing facility in 2007 and since that time it becomes to produce the marketing goods itself. Although it is a new company in manufacturing, it does not take so much time to begin the production of hydrophilic catheter in the world standard due to its wide knowledge of industry and also experienced team. Because of the consciousness how important is the quality and scientific support in production, it has achieved to take R&D support of the scientific organizations such as TUBITAK Turkish Scientific and Technical Research Institution and SAN-TEZ by Turkish Ministry of Industry & Trade. Moreover, the leading support of technology partners in principal universities made serious contribution to our strength. Today Istem Medikal has become the leader of the sector which has also started to export aiming to get the first place in the international arena . Therefore our initial goal is to study more and more for human health protection for both Turkey and worldwide. With this respect ,it becomes our principle to improve the quality of our products and to maintain self-development with increasing product variety groups every year. Our vision is to accelerate the development of health sector doing the best that we can . We realize it without sacrificing our quality. Furthermore, we encourage our production department with training programmes. We also follow the development in automation technology step by step and apply it to our production systems. We have performed a first in the production of hydrophilic catheter. We generate our own resources and use them in all phases of production thus we created a production department. ISTEM MEDICAL that has EN ISO 9001:2015 and EN ISO: 13485:2016 quality certificates aims to be the pioneer in the sector. ?stem Medikal has been granted following quality certificates; ISO 9001 : 2015 ISO 13485 : 2016 CE QUALITY MANAGEMENT SYSTEM CERTIFICATES Class I SterIle Class IIa Class IIb CE DESIGN EXAMINATION CERTIFICATES Class III Istem Medikal has registered trademarks and has some international patents rights of the technologies that she developed.
IBI Istituto Biochimico Italiano G. Lorenzini S.p.A. is an independent Italian research-based pharmaceutical company pioneer since 1918 in the development, production and marketing of medicines worldwide. Following our mission of “creating to contribute”, we have used innovative technology to develop a portfolio of products to improve the health of patients. IBI is present has an established leadership in penicillin market and capability of aseptic filling for injectable drug products aimed for different therapeutic areas. IBI's high quality standards is internationally recognized by the most demanding health authorities : AIFA, US FDA, EDQM, TGA and PMDA. R&D is one of the strengths of the Istituto Biochimico Italiano. Thanks to the fact that many manufacturing processes have been developed entirely in house; from the semi synthesis of active substances (ß-lactam) to the development of the formulations, the company has obtained numerous patents. Investment in resources and in innovative equipment enables us to continuously improve production and analytical processes.
We aim to be the preferred supplier of vitamins and nutritional supplements. Our history of supplements manufacturing can be traced back to 1997 when we successfully launched our first dietary supplement – Aland® (national brand) Vitamin C Chewable Tablet in China. With the booming of the sales we broaden our vision and decide to expand our business abroad.
Our products include Private brand and contract manufactured bulk nutritional supplement tablets, capsules and powder for domestic and international markets.