Exhibitors

IN India
Stand No: 3H33
New
Location:
Sub-event: ICSE18
Zone: NEP ICSE
ES Spain
Stand No: 3H70
New
Asphalion is an international Scientific and Regulatory Affairs consultancy, with offices in Barcelona and Munich. We collaborate with Pharma and Biotech companies facilitating Drug Development and Regulatory Affairs projects for Drugs, Biologics, Biosimilars, ATMPs and Medical Devices. Our involvement ranges from early development, through to registration and post-commercialization phases. Since the company was founded in 2000, we have consistently grown and now have a team of over 80 employees with backgrounds in all areas of life sciences. Our consultants are experts in their fields and are in direct contact with European agencies for the implementation of new regulatory standards. We provide global services and work for hundreds of clients from around the world. Through collaborations with partners in all other continents, we can accelerate your worldwide scientific and regulatory activities by using local expertise. Services: · Regulatory and Scientific Strategy during Development · Medical and Scientific Writing · Global Submissions...
Location:
Sub-event: ICSE18
Zone: NEP ICSE
ES Spain
Stand No: 3G60
New
Location:
Sub-event: ICSE18
Zone: NEP ICSE
ES Spain
Stand No: 3G60
New
Azierta is a Science and Health consultancy firm committed to strengthening bonds between science and the business environment through the “Science to Business” concept. We provide services in the field of medicinal products, Medical Devices, cosmetics, food supplements and biocides, offering complete solutions throughout products' life cycle, from medical and regulatory support, to toxicology, manufacturing and distribution needs, market access and pharmacovigilance. We have collaborated with more than 300 clients in the European environment through a multidisciplinary expert team, always focused on results and taking into account the needs of our customers. Services: European Market Access Support Services, Full Regulatory Affairs Support, Dossiers action plan, GMP Compliance Status Assessment, Pharmacovigilance services, Bioequivalence studies aligned with all EU requirements, Analytical support, Support for EU drugs auctions/tenders, Search of customers and sales networks, European Compliance Support services, Characterization of toxicological impurities, ERA (Environmental Risk assessment).
Location:
Sub-event: ICSE18
Zone: NEP ICSE
BE Belgium
Stand No: 3H64
New
C.E.L.forPharma - the Centre for Executive Leadership for the Pharmaceutical Industry – is the only international institution where PHARMA, BIOTECH & MEDTECH executives in market-facing functions can learn business critical competencies from top-notch international experts in the fields of: Business Development & Licensing – Market Access – Medical Affairs – Pharma Marketing. Attending a 1- or 2-day C.E.L.forPharma course equips you and your company with state-of-the-art market-oriented competencies to better manage business processes that lead to success in pharmaceutical markets. C.E.L.forPharmacourses offer unique opportunities to discuss issues and exchange ideas with peers from other companies and/or countries.
Location:
Sub-event: ICSE18
Zone: NEP ICSE
IT Italy
Stand No: 3F61
New
Pure CDMO for third parties. Food supplements: granulates, powders ( also oro-soluble), capsules, tablets: effervescent, simple and coated, double and triple-layer, controlled-release, chewable, mono and multidose liquids, alcoholic products - Lic.U.T.F. Lquid packaging: bottles, liquid monodose vials with and without plug cap for powders, minidrinks, syrups, drops, sprays. Solid packaging: blister, strips, sachets,stick pack, bottles. Probiotics: in dedicated and isolated area ( sachets, stick packs, capsules, tablets and drops). Cosmetics: creams, gels, solution and emulsions. Medical devices: solid, liquid and semisolid forms for oral and topic use. Highly qualified personnel - Advanced equipment -Production areas in class ISO 8 to guarantee the safety of products Certifications: ISO 9001:2015- ISO 13485:2016- GMP according to FDA 21 CFR part 111 - IFS Food Version 6 - ISO 14001: 2015 - OHSAS 18001: 2007
Location:
Sub-event: ICSE18
Zone: NEP ICSE
US United States
Stand No: 3H35
New
Location:
Sub-event: ICSE18
Zone: NEP ICSE
CN China
Stand No: 3G71
New
Established in August 2011, Raffles PharmaTech is a high-tech enterprise that focus on development, manufacturing and sales of high-value added active pharmaceutical ingredients and intermediates. We are specialized in applying organic catalysts into the process development to lower cost, and to provide cost-effective product and service to customers.
Location:
Sub-event: ICSE18
Zone: NEP ICSE
IT Italy
Stand No: 3H32
New
Location:
Sub-event: ICSE18
Zone: NEP ICSE
LV Latvia
Stand No: 3G70
New
Location:
Sub-event: ICSE18
Zone: NEP ICSE
GR Greece
Stand No: 3H50
New
Laboserve is an independent, international pharmaceutical company with its own, brand new manufacturing site, headquartered in Athens, Greece. Representing our Clients, we offer licensing rights of differentiated, added value generic products, products with unique presentations and drug combinations, protected with proprietary patents. In addition, our specialized pain management portfolio addresses moderate to severe pain through immediate release, oral liquid dosage forms of controlled substances. We offer: Out-licensing opportunities FDF contract manufacturing services in our EU-GMP site We are interested in partnering and out-licensing of our Client's dossiers to third parties with supply agreements.
Location:
Sub-event: ICSE18
Zone: NEP ICSE
TH Thailand
Stand No: 3H37
New
Medica Innova (We), established in late 2006 and located in Bangkok, is the first Thai own "Contact Research Organization (CRO) Plus" providing drug development services to Thai and International Pharmaceutical companies. We have now officially received OECD-GLP Compliance Status, recognized by Bureau of Laboratory Quality Standards, Department of Medical Sciences, Ministry of Public Health, Thailand. In addition, we have been approved to be in the list of NPRA Compliance Programme for BE centers in Malaysia. We would like to take this opportunity to introduce one of our areas of expertise, we have a broad knowledge and experience in Clinical Development from Phase I-IV including BA/BE studies. At Medica Innova, all clinical trials including the BA/BE studies are conducted in compliance with the Good Clinical Practice (GCP) to ensure the quality of the trials especially the right, safety and well-being of subjects as well as the data credibility. Furthermore, we have...
Location:
Sub-event: ICSE18
Zone: NEP ICSE
GB United Kingdom
Stand No: 3G63
New
NSF International specializes in helping pharmaceutical and biotech manufacturers grow through our world-class training, consulting and auditing services. Whether you are trying to get a product to market faster, keep it compliant or get out of trouble with a regulatory body – you can rely on NSF's expertise. We work with companies of all sizes. Whether you are a start-up or a multinational manufacturer, we help make sure your product lines are fully compliant with the toughest and latest standards. NSF provides comprehensive services in three key service areas: Consulting Auditing Training and Education
Location:
Sub-event: ICSE18
Zone: NEP ICSE
VN Vietnam
Stand No: 3H60
New
SAVIPHARM J.S.C certified Japan GMP is a leading pharmaceutical manufacturer in Vietnam, a leading contract manufacturer of GSK to manufacture and supply pharmaceuticals to Japan and ASEAN countries. SVP is willing to cooperate with partners in manufacture and supply of pharmaceuticals, franchising, technology transfer, toll manufacture, R&D of new products.
Location:
Sub-event: ICSE18
Zone: NEP ICSE
NL Netherlands
Stand No: 3H51
Tjoapack is a global contract packaging organisation (CPO) specialising in primary and secondary pharmaceutical packaging and supply chain management services. We're dedicated to shaping the future of the pharmaceutical supply chain to be safer and more reliable for our customers and for patients. With almost 30 years' track record in contract packaging, we use our knowledge and experience to offer flexible solutions to our customers challenges, and use the latest technologies to continuously improve our operations. We now supply products to over 40 countries across all continents.
Location:
Sub-event: ICSE18
Zone: NEP ICSE
US United States
Stand No: 3H52
New
UPM Pharmaceuticals is a Bristol, Tennessee-based independent contract development and manufacturing organization (CDMO) serving the pharmaceutical and biotechnology industries. UPM provides high quality pharmaceutical drug development services that include formulation development, cGMP manufacturing and packaging, analytical method development and testing from concept through commercialization.
Location:
Sub-event: ICSE18
Zone: NEP ICSE