Exhibitors

US United States
Stand No: 3C60
AbbVie Contract Manufacturing has a portfolio of state-of-the-art facilities, offering a broad range of capabilities in North America and Europe. For more than 30 years, AbbVie Contract Manufacturing has offered contract manufacturing services that spans biologics, potent, drug product, prefilled syringes, fermentation, as well as selling high quality active pharmaceutical ingredients (APIs).
Location:
FI Finland
Stand No: 12A24
New
Admescope is a CRO providing the pharmaceutical industry with tailor-made ADME-Tox services. Our unique expertise lies in drug metabolism, drug-drug interactions, pharmacokinetics and quantitative bioanalysis. Our service portfolio covers assays for small molecules, peptides and biopharmaceuticals. At the moment, we serve customers in 24 countries on 4 continents.
Location:
Sub-event: BIO18
APL is a leading Scandinavian CDMO in the Life Science sector with resources for development, manufacturing and analysis of pharmaceuticals. APL mission is to manufacture personalised medicines tailored to patients with specific needs. 550 employees at four production facilities in Sweden contribute to an annual turnover of about 150 M€.
Location:
BE Belgium
Stand No: 3A1
We are Ardena, a reputable contract partner delivering drug development, manufacturing, logistics and (bio)analytical services to pharmaceutical customers globally. In parallel, we work with you to compile your regulatory dossier and to fast track your product towards compliance. Every day, we guide companies through the hurdles and challenges of drug development. Our integrated service offering helps to streamline the drug's progress to clinic and beyond. Ardena is your one source contractor for the chemical and pharmaceutical development of your valued compounds. In parallel, we provide you with full product analytical and bioanalytical support during development. Our dossier centric approach makes a difference. We work with you to compile your regulatory dossier in parallel with drug development, saving you time, identifying hurdles and fast tracking your product to compliance. We are experts in writing and formatting supporting CMC documentation.
Location:
DE Germany
Stand No: 12B33
New
Driven by content, focused on results Biotechnology, medical technology, bioeconomy – these terms are watchwords of optimism and hope for all mankind. Backed up by policies and capital, cutting-edge science and research are constantly redrawing the map of what we know. Companies are eager to bring the latest technology to the market, society and people. In every step along the way, effective communication can mean the difference between success and failure. For almost 30 years, BIOCOM AG's top-notch industry experts and reporters have guided and supported life sciences customers on the path from the lab bench to the market. Driven by content and focused on results, we supply the expertise and enthusiasm that make our client's projects work. https://biocom.de/en/ https://european-biotechnology.com/ https://medtech-zwo.de/ https://transkript.de/ https://laborwelt.de/
Location:
Sub-event: BIO18
US United States
Stand No: 3D10
Catalyst + Talent Our name combines these ideas. From drug and biologic development services to delivery technologies to supply solutions, we are the catalyst for your success. With over 75 years of experience, we have the deepest expertise, the broadest offerings, and the most innovative technologies to help you get more molecules to market faster, enhance product performance, and provide superior, reliable manufacturing results. We serve thousands of innovators, large and small, in over 100 markets, including 36 of the top 50 biotech companies and 49 of the top 50 pharmaceutical companies. Our team of over 1,000 talented scientists supports 40% of recent new drug approvals, and our nearly 30 global sites make or package over 100 billion units annually. Our significant intellectual property in oral, injectable, and respiratory dosage forms and advanced drug packaging includes over 1,200 patents and patent applications.
Location:
FR France
Stand No: 1J30
Our mission: To assist you in the development and control of your products To provide a technical & regulatory support Cebiphar, French CRO member of TERANGA Group (100 employees), offers its expertise to the pharmaceutical, chemical, veterinary and cosmetics industry. This expertise encompasses 4 strategic activities: Development and control Stability studies Veterinary preclinical and clinical studies Technical and regulatory affairs Member of TERANGA Group, Cebiphar offers relevant synergies with its sister companies : ACM Pharma with regards to microbiological services UPS Consultants with regards to training sessions. Cebiphar in figures : nearly 40 years experience, more than 2000 products being studied, 1000 veterinary preclinical & clinical studies. More than 150 clients work with us on a regular basis, in France and internationally: start-up, big pharma, generic companies, API producers, cosmetic producers. Cebiphar's sustained commitment to quality enables the performance of studies according to GMP, GLP and GCP quality standards. Cebiphar benefits from the Research Credit Tax certification.
Location:
US United States
Stand No: 6A50
Clarivate Analytics accelerates the pace of innovation by providing trusted insights and analytics to customers around the world, enabling them to discover, protect and commercialize new ideas faster. We own and operate a collection of leading subscription-based services focused on scientific and academic research, patent analytics and regulatory standards, pharmaceutical and biotech intelligence, trademark protection, domain brand protection and intellectual property management. Clarivate Analytics is now an independent company with over 4,000 employees, operating in more than 100 countries and owns well?known brands that include Web of Science, Cortellis, Derwent, CompuMark, MarkMonitor and Techstreet, among others. For more information, visitclarivate.com.
Location:
Sub-event: CPWW18
Zone: API
US United States
Stand No: 1G97
Contract Pharma is the international magazine for pharmaceutical and biopharmaceutical outsourcing. With over 20,000 BPA qualified subscribers, we offer a print and digital magazine, weekly e-newsletter, an annual company profile and contract services directory, an annual Conference and Exhibition and website with the latest breaking news. Stop by our stand for your FREE subscription today.
Location:
Sub-event: ICSE18
FR France
Stand No: 1J30
A 25 years pharmaceutical company specialized in: - Clinical supplies: support to pharmaceuticals/biotech companies in their Phase I to IV clinical trials, from comparator sourcing to worldwide logistics, through primary & secondary packaging - Customized Manufacturing Operations: packing, repacking & distribution of drug products and food supplements, without minimal batch size
Location:
IT Italy
Stand No: 4D53
CSV Life Science serve the pharmaceutical market with engineering and construction solutions. Our services: Facility planning, engineering design, construction, equipment and plant validation, and computer system validation. CSV Life Science is the exclusive agent in Italy, Malta and South Africa for ILC Dover: specific applications based on flexible technology, custom-tailor and studied for containing high potent drugs (safety), and creating classified (GMP) or humidity controlled areas surrounding exposed operations in contamination background. In last years, CSV Life Science started to re-define the group experience: CSV Active and CSV Construction are the newest companies of the group, with a core business in intermediates and API trading and in construction management respectively.
Location:
Sub-event: ICSE18
Zone: PMEC
GB United Kingdom
Stand No: 9J40
The Department for International Trade is the UK Government department responsible for promoting British trade across the world. We provide operational support for exports as well as facilitating inward and outward investment. Visit stand 9J40 to learn more on UK capability in the chemical and pharmaceutical manufacturing sector.
Location:
LV Latvia
Stand No: 3G70
New
Dokumeds is mid-size CRO with 10 registered offices across Europe and Russia, operating globally, together with strategic partners. We are trusted partner for pharmaceutical and biotech companies, managing phase I–IV clinical trials. Dokumeds strength is our professional and dedicated team who will execute your project smoothly, reach recruitment targets, and ensure quality-focused oversight.
Location:
Sub-event: ICSE18
Zone: NEP ICSE
IT Italy
Stand No: 1G62
New
GB Pharma Group is an international CRO, Quality Assurance ,Pharmacovigilance and Regulatory Affairs consultancy company, with offices in Barcelona and Lugano, Pavia (near Milano) and Rome .We collaborate with Pharma and Biotech companies facilitating Clinical Drug Development and Regulatory Affairs projects for Drugs, Biologics, Biosimilars, and Medical Devices. Our involvement ranges from early development to registration and post-commercialization phases. Since the company was founded in 2001, we have consistently grown and now have a team of over 60 employees with backgrounds in all areas of life sciences including experts from non-clinical, clinical operations, CMC, project management and regulatory affairs.We provide global services and work for many clients around the world. Through collaborations with partners in all other continents, we can accelerate your worldwide clinical and regulatory activities by using local expertise. We are also Marketing Authorization Holders experts in rare disease. On the top of this, we can be defined...
Location:
DE Germany
Stand No: 3G101
GBA Pharma is a service provider for pharmaceutical companies and is supporting research & development as well as services in the commercial stage. Our success and opportunities is based on a high qualified staff. The headcount of GBA Pharma represents 200 employees distributed over 5 locations in Europe with +50% academic staff. Our portfolio comprises the following service areas: Contract research in the preclinical arena (in vitro & in vivo) Pharmaceutical testing under GMP incl. stability study services & QP release services Bioanalysis under GLP: in vivo toxicology studies and phase-I/II clinical studies GMP qualification of API and drug manufacturer outside the European Union Distribution and clinical trial supply management for multicentre trials Consultancy & regulatory affairs with regard to GMP, GLP & GCP We would be delighted to develop a tailored solution for you.
Location:
DE Germany
Stand No: 6C10
Gen-Plus is a privately-owned company located in Munich. We develop formulation and technology concepts for pharmaceutical industries (NCE, value-added-Generics, OTC). This includes solid/semisolids, patches and thin films from early idea to IMP production under GMP. Further in-house capabilities: narcotics&high potent handling (isolators), high-tech analytics incl. skin permeation testing, 2D/3D-API-printing.
Location:
Sub-event: CPWW18
Zone: API
IN India
Stand No: 7F31B
GLOBAL PHARMA a finished pharmaceutical formulation manufacturer - WHO cGMP and designed to qualify for EU –GMP& PIC/s. Currently exporting to 30 countries .Manufacturing Solid orals, Topicals, Sterile preparations in all therapeutic segments .
Location:
Sub-event: CPWW18
GB United Kingdom
Stand No: 1D91
At GMP Compliance LTD we are a team of highly skilled and passionate individuals who together offer a valuable support and consultancy service to the pharmaceutical and food supplement industry in regards to Good Manufacturing Practice. We truly love what we do. We get it right in an industry where getting it wrong is not an option. Our clients feel secure in the knowledge that we have the right experience, qualifications and drive to deliver the right results. GMP Compliance LTD offer support and guidance by providing the following services:Validation Services: Computer Systems, Documentation Systems, Equipment, URS/IQ/OQ/PQ generation, Project Management, Method. Audit Services: IRCA Certified Lead Auditors, API, QP, CMO, Packaging, Pre Inspection, Gap Analysis, Cosmetic, Medical Device, ISO, Computer Systems, GMDP, GCP, PV. PQS Services: Documentation Support, QA Support, Contract QP/RP, Production Advice, Self Inspections. Technical Services: Technical Transfer, Project Management, Supplier Sourcing, Regulatory Support, Licensing Support, Excipient Risk...
Location:
IN India
Stand No: 5B14
Hikal is a reliable long-term outsourcing partner and supplier of key active ingredients and intermediates to companies in the Pharmaceuticals, Crop Protection and Specialty Chemicals industry. Our advanced manufacturing facilities have been certified by the US FDA, MHRA, EDQM, COFEPRIS,TGA, and are ISO 9001:2008, ISO 14001 and OHSAS 18001 certified. Strengths: Supply and Regulatory support on Generic APIs, Custom Synthesis; Contract manufacturing; Process development and Scale-up expertise; Respect for Intellectual Property. Hikal has five state-of-the-art manufacturing facilities in India at Maharashtra (Taloja and Mahad), Gujarat (Panoli) and Bangalore (Jigani) including an R&D centre and a state-of-the art R&D centre at Pune
Location:
Sub-event: CPWW18
Zone: API
AT Austria
Stand No: 3D73
Human.technology Styria (HTS) has been founded in 2004 as a cluster organization with a focus on health technologies. Placing the human beings in the centre of all considerations, the HTS and its members are inventing and improving technologies, products, and services that enhance the human development and health. Currently, the cluster has approx. 115 members, from all areas in life science and related industries. Human.technology Styria strives to bundle capabilities, utilize synergies, initiate new projects, strengthen the innovative spirit and optimize the international visibility of our Partners, in order to support their success on the international forefront of innovation. The HTS has developed two areas of strength with the vision to create an added value for our members: medical technologies and pharma & biotechnology. Regarding MedTech, the HTS supports companies and research institutions, active in medical (micro)electronics, production technologies like precision mechanics or injection moulding, materials expertise, automation, biomedical sensor...
Location:
DE Germany
Stand No: 14.1C93
As a service provider for the pharmaceutical industry, Jesalis Pharma exports pharmaceutical products manufactured in Germany to non-European countries. Jesalis is particularly strong in handling the whole chain from market research to distributor retrieval to registration adaptation to commercial, logistical and legal processing of export to even pharmacovigilance.
Location:
ES Spain
Stand No: 14.0H84
Kymos is a reliable CRO, certified in GLP and GMP with laboratories in Spain and Italy. Kymos provides contract research, development and analytical services for pharmaceutical, biotechnology, veterinary, fine chemistry, cosmetics and nutraceuticals industries. The main areas of activity are: i) batch testing, batch release and importing of medicinal drug products for human, veterinary and investigational use in the EU; ii) quality control of raw materials and finished drug products, analytical development and validation, stability studies, microbiological testing and PAT-QbD consultancy; iii) biopharmaceutical testing of proteins an monoclonal antibodies and comparability of biosimilars; iv) immunogenicity testing, cell based assays and bioanalysis of biologics and small molecules, including full management o bioequivalence studies.
Location:
IT Italy
Stand No: 1G50
Labomar is a research, development and manufacturing company devoted to innovation in food supplements, medical devices, foods for special medical purposes and cosmetics; it offers a full service throughout the different development phases. Labomar R&D Department designs innovative patents that ensure more effective delivery systems. Labomar has also a licensing product line Certifications and Compliances ISO 9001:2008 ISO 13485:2012 GMP Nutritional Supplements .
Location:
IN India
Stand No: 14.0H73
Lambda Therapeutic Research, is a leading global CRO, with strategic locations in India, Europe, UK & North America, offering full spectrum of services in the most efficient yet cost effective way:Phase I–IVPatient based Pharmacokinetic studies BA/BEPharmacovigilanceBiosimilar capabilitiesBioanalyticalData ManagementMedical Imaging21 CFR Part 11 compliant software solutions for:PV Safety DatabaseGlobal Regulatory Submission Clinical Trials Management
Location:
Sub-event: FDF18
GB United Kingdom
Stand No: 3H71
LGC is an international life sciences measurement and testing company. Operating from state-of-the-art facilities to GLP, GCP and cGMP standards, LGC has leading capabilities in CMC, with particular specialties in materials science and pharmaceutical analysis. In support of the development and manufacturing of small and large molecule drugs, LGC provides method development, ICH validation and routine testing services. We offer unknown impurity determination, structure elucidation, compatibility studies, stability storage and testing. We are a leading provider of extractables and leachables studies and elemental impurity analysis. Our World-class material characterisation capability supports formulation development and manufacturing. LGC also has a state of the art bioanalytical capability in high-integrity analytical science and expertise spanning small and large molecules, biomarkers and molecular biology.
Location:
CN China
Stand No: 12H21
Luye Pharma Group Ltd., an investment holding company, develops, produces, markets, and sells pharmaceutical products. The company offers Maitongna for cerebral edema and edema caused by trauma; Xuezhikang, a blood lipid regulator capsule; Tiandida for ovarian or non-small cell lung cancer; Yitaida for acute promyelocytic leukemia and liver cancer; CMNa for tumor radiotherapy; and LIPUSU for ovarian, metastatic ovarian, breast, and non-small-cell lung cancer patients. It also provides Nuosen for acute upper digestive tract hemorrhage; Bei Tang Ning, a capsule to control blood glucose in patients with type 2 diabetes; Bei Xi, an acarbose capsule for diabetes; and LUTINGNUO, reduced glutathione injection for toxicity, liver damage, and injuries caused by ionizing radiation, as well as for hypoxemia. In addition, the company offers Glucosamine Hydrochloride tablets for osteoarthritis; Xi Ming Ting largetrifoliolious bugbane rhizome total saponin tablets for invigorating splenic yang and relieving depression, and treating perimenopausal syndrome in females, as...
Location:
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
AT Austria
Stand No: 3D73
NP&D is a developer, producer and distributor of nutritional / food supplements for joints, back, spinal discs, prostrate, osteoporosis, etc. Our brand portfolio includes Arthrobene, vertebene, Biobene and Primabene. We are also supplier and distributor of raw ingredients with its focus on plant/vegetable oils and fats for cosmetics and nutrition. We are looking for distributors of our nutritional supplement lines.
Location:
DE Germany
Stand No: 3A102
New
As a partner for the industry, Navitas Life Sciences leverages industry insights, consulting and technology capabilities to deliver full service clinical, regulatory and safety solutions and desired outcomes to our clients. Navitas Life Sciences, the dedicated life sciences company of TAKE Solutions, harnesses the combined knowledge and experience of three legacy companies—Ecron Acunova, Navitas, and Intelent—to provide end-to-end services and solutions. We help our clients address their most critical problems by bringing together the capabilities of a full-service CRO, a technology-led life sciences services provider across clinical, regulatory and safety, and a life sciences big data services and analytics provider. With a rich legacy of experience in life sciences, we have worked with 9 of the top 10 global pharma companies.
Location:
ES Spain
Stand No: 3C92
CDMO partner based in the EU, highly specialized in Biologics (proteins, mAbs,…) and Cell Therapies, providing development and fill and finish, including lyophilization, for clinical batches and commercial supply of high value sterile drugs. Vials and plastic bottles filling.
Location:
IN India
Stand No: 3A83
Raptim Research Ltd. is a quality-oriented full-service contract (clinical) research organization. Raptim provides end-to-end services to global Pharmaceutical (generic as well as research-based), Biotechnology and Cosmetic industry. The studies done at Raptim are globally submitted and approved by various regulatory agencies including USFDA, EMA, UK MHRA, Canada (TPD), WHO and etc. Raptim Research Ltd., incorporated in the year 2005, has its facilities based in Navi Mumbai and Business Office in Navi Mumbai as well as New Jersey, USA. Raptim is leader following activities: Bioequivalence / Bioavailability Studies (BE/BA studies) PK end-point studies PD end-point studies Clinical trials – phase II & IV Studies on Special Population Apart from the above, Raptim has developed expertise in niche area of drug development and has pioneered in testing/screening Dermal Topical Products including Cosmetic Products as well as inhalation products. These include: In vitro Release/Permeation (IVRT/IVPT) studies In vivo – Tape Stripping studies In...
Location:
SE Sweden
Stand No: 3D50
Recipharm is a leading contract development and manufacturing organisation (CDMO) headquartered in Stockholm, Sweden. We operate development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK and the US and are continuing to grow and expand our offering for our customers. Employing around 5,000 people, we are focused on supporting pharmaceutical companies with our full service offering, taking products from early development through to commercial production. For over 20 years we have been there for our clients throughout the entire product lifecycle, providing pharmaceutical expertise and managing complexity, time and time again. Despite our growing global footprint, we conduct our business as we always have and continue to deliver value for money with each customer's needs firmly at the heart of all that we do. That's the Recipharm way. For more information visit www.recipharm.com
Location:
KR South Korea
Stand No: 12C14
New
Samsung Biologics provides one-stop service from cell-line development, process development, Tox & Clinical material, and commercial manufacturing of Drug Substancee & Drug Product at the same site.
Location:
Sub-event: BIO18
AT Austria
Stand No: 6C20
Sandoz GmbH develops and manufactures healthcare products. Its product line includes bio-similars, inhalers, patches, injectables, and oral solids. The company was formerly known as Biochemie GmbH. The company was founded in 1946 and is based in Kundl, Austria. Sandoz GmbH operates as a subsidiary of Sandoz International GmbH.
Location:
Sub-event: CPWW18
Zone: API
DE Germany
Stand No: 4G80
We deliver and implement rapid and cost-effective Biomanufacturing solutions from early phase development through scale-up to commercial manufacturing. Benefit from the most comprehensive bioprocess technology portfolio coupled with our expertise in Single-use bioprocess engineering. Our global bioprocess teams are available to discuss your process development and manufacturing requirements.
Location:
Sub-event: ICSE18
Zone: PMEC
US United States
Stand No: 3G90
Our Life Science Services provide analytical, bioanalytical and clinical trial testing capabilities, along with process management, that enable pharmaceuticals to swiftly reach those that need them with minimal cost and maximum safety. We partner with the pharmaceutical, biopharmaceutical, biotechnology, medical device and healthcare-related industries to provide a wide range of essential services.
Location:
NL Netherlands
Stand No: 3H30
Sharp Packaging Services, a division of UDG healthcare, is a global leader in contract packaging and clinical services. Operating from state-of-the-art facilities across the US and Europe, Sharp has built an international reputation for delivering cost-effective blister packaging, bottling, pouches and stick packs, compliance packaging, formulation and manufacturing services, label design and printing. Sharp is also a world leader in 'Track and Trace' serialization services, which will require all prescription drugs to have a unique serial code for authentication and traceability.
Location:
Benepure is a global researcher, manufacturer and supplier of botanical extracts, active pharmaceutical ingredients&intermadiates, pigments&flavours used for pharmaceutical, nutrition food, cosmetics, etc. It owns strong research and development team, cutting-edge equipment, high-standard manufacturing base and philosophy of professional service, devoted to offering new products and innovative services in varied fields of pharmaceutical, functional food, cosmetics and feed industries. Our objective: we strive to provide high-standard products and professional services with higher efficiency and more convenience . we'll never stop trying for humans' health. Any interesting, please feel free to contact with us at [email protected] , or call us at +86(28)86799990.
Location:
Sub-event: CPWW18
CH Switzerland
Stand No: 3A22
Solvias is a world leader in contract research, development and manufacturing. The industries we serve include pharmaceuticals, biotech, medical devices, cosmetics, chemical, electronic materials, life sciences and oil. Solvias is a management- and employee-owned company headquartered near Basel, Switzerland. Our team of over 400 highly-qualified employees work closely together to find solutions that fulfill your requirements. We take pride in delivering the best quality and results for our customers. Our excellent infrastructure and unrivalled expertise ensure you can rely on us to move your substances and products forward. With a well-established scientific experience and proven track record, we provide integrated services, products and technologies to enhance the value chain for customers worldwide. Our service portfolio covers: Analytical Services Small Molecule Analysis Biopharmaceutical Analysis Solid-State Development Microbiology & Biological Analysis Ligands & Catalyst Technology Custom Synthesis & Manufacturing
Location:
Sub-event: ICSE18
NL Netherlands
Stand No: 12F44
New
Sonoma Pharmaceuticals is a specialty pharmaceutical company dedicated to identifying, developing and commercializing unique, differentiated therapies. Sonoma Pharmaceutical's portfolio features unique technology and products to help manage Wound Care, Oral Care, Eye Care and Dermatological discomforts like eczema, atopic dermatitis, acne and scars. Unique Anti-in?ammatory-, Antimicrobial-, pH Neutral-, non-Toxic & non-Cytotoxic technology. Non-Irritating, non-Staining and Safe. Our products do not induce bacterial resistance and support the body's own healing process. Sonoma Pharmaceuticals is partnered with industry-leading partners in more than 50 countries and is bringing to market unique evidence based, differentiated, patent-protected and high-quality CE-marked products that are affordable, efficacious and accessible to most every patient.
Location:
FR France
Stand No: 2F40
Stiplastics has been creating, developing and producing plastics solutions for the pharmaceutical industries and the health sector since 1985. Stiplastics comprises three separate Business Units, each devoted to one of the group's fields of expertise. Stimed offers standard dosing products (droppers, cups, spoons, cannulas, etc.) and develops custom primary and secondary pharmaceutical packaging solutions that can be manufactured based on a set of specifications or created from A to Z based simply on a need or idea expressed by the client. Sticare offers its own brands of family health products in the form of the Pilbox® and Doseo®pillboxes. Its Hemobox® biological sample transportation solution and its VisionAIR® Plus respiratory range. Stitech benefits from the long-standing expertise that Stiplastics has developed in the manufacturing of industrial technical parts. Stiplastics strives to facilitate and improvethe day-to-day lives of those who use its products. With this in mind, we can advise on and...
Location:
Sub-event: IP2018
Zone: InnoPack
IN India
Stand No: 3C100
Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), an innovation focused global discovery, development and manufacturing organization provides integrated services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemicals industries across the world. Syngene's clientele include market leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Zoetis, Merck KGaA and Herbalife. Its innovative culture is driven by a strong team of over 3500 scientists working with clients around the world to improve R&D productivity, while reducing development time and cost. For more details, visit www.syngeneintl.com .
Location:
TW Taiwan
Stand No: 9A70
Taiwan Pharmaceutical Alliance (TPA) comprises several Taiwan-based manufacturers, including API & FDF (chemicals & biologics). TPA facilities pass PIC/S GMP. Products are marketed in US, EU, Japan & ASEAN etc. TPA provides quality products with affordable price. Niche products include liposome & microsphere, OROS Tablets/ ODT, high potent soft gel, MDI/DPI, eye drops, patch, biosimilar etc. Services include CDMO/CMO, license in/out, and trading etc. TPA is your trustworthy partner in the dynamic markets.
Location:
ES Spain
Stand No: 3H74
TECNALIA Pharma Labs is a full-service Contract Development, Manufacturing Organization (CDMO) that provides high quality services under a strong quality system, with over two decades serving the pharmaceutical industry. We provide comprehensive services across the entire value chain (human medicines, medical devices, food supplements, cosmetics & veterinary medicines). • Pharmaceutical development: Galenic & Analytical Development, Stability Studies • Clinical Trials: Bioequivalence Studies, Phase I, II, III & IV Clinical Trials, Nutritional Clinical Studies. • Manufacturing: Contract Manufacturing of Industrial Batches for third parties • Pharmacogenetics. TECNALIA also offers development and efficacy assessment of Pharmaceutical OTC products against blood-sucking arthropods.
Location:
Sub-event: ICSE18
BE Belgium
Stand No: 2C10
Terumo Pharmaceutical Solutions Carefully Crafted We develop alliances with pharmaceutical companies on a global scale, using Terumo technology to develop, manufacture and supply carefully crafted solutions to their injectable drug delivery challenges. We pride ourselves on offering a full portfolio of products and services for the pharmaceutical industry, backed by unrivalled scientific expertise and know-how. By anticipating new trends and maintaining a constant dialogue, we provide a first class customer experience.
Location:
Sub-event: IP2018
Zone: InnoPack
DE Germany
Stand No: 1J52
tesa Labtec – Your innovation driven CDMO for transdermal patches and thin films tesa Labtec offers the development and manufacture of film shaped dosage forms (CDMO services) such as transdermal and topical patches as well as oral, buccal or sublingual films. The business activities comprise formulation development, scale up and manufacture of clinical trial supplies or finished products under full cGMP conditions. tesa Labtec counts on its proprietary technologies Transfilm®, Rapidfilm® and Mucofilm® allowing to deliver not only small molecules but also peptides, vaccines and allergenes. tesa Labtec is a wholly owned subsidiary of tesa SE, a member of the Beiersdorf group of companies, and offers its services to customer worldwide. tesa is EU cGMP certified and also has passed an US FDA pre-approval inspection in 2016.
Location:
Thermolab Scientific Equipments Pvt Ltd is the flagship company of the Thermolab Group. It was established in 1967 and this year we complete 50 years. It has been a remarkable journey for us. It is one of the leading manufacturers for a variety of stability chambers, cooling cabinets, incubators, and ovens; in all possible capacities for its customers across the globe.
Location:
Sub-event: ICSE18
Zone: PMEC
MX Mexico
Stand No: 14.0B60
The Health Research Unit, Unidad de Investigación en Salud® (UIS®), is a Mexican business Group that, since 2005, has worked around research for the benefit of human beings. Our commitment is to offer Services for science (Servicios para la ciencia®). We provide clinical sites for testing new drugs in sick people and clinical unit for bioequivalence tests in healthy people. Other services include ethical review, training, project management and software development. We also participate in markets related with health through patent trade.
Location:
Sub-event: FDF18
DE Germany
Stand No: 3C80
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.
Location:
AT Austria
Stand No: 3D73
Pichia pastoris Protein Expression / Production Excellence Be competitive with high-quality proteins, high-productivity strains & robust and scalable bioprocesses from world´s broadest Pichia pastoris protein production toolbox VTU Technology is a leading contract research and development company, providing time-saving development of cost-efficient recombinant protein production processes for manufacturing of biologics and other proteins Cutting-edge, exclusive, proprietary technologies and extensive know-how are the basis for the broadest toolbox and most versatile technology platform available for Pichia pastoris recombinant protein expression / production enabling highest productivities of up to 25 g/L of secreted protein (peak productivity of 35 g/L) for e.g. cytokines, growth factors, hormones, serum proteins to fusion proteins (Fc-and albumin fusion), protein scaffolds, antibody fragments and vaccine antigens, enzymes or allergens. VTU guarantees tight development timelines and competitive & safe production processes. Unlock Pichia - VTU Technology´s toolbox: Exclusive AOX1 promoter libraries Diverse set of platform strains Proprietary expression enhancing...
Location:
GB United Kingdom
Stand No: 3A75
World Courier is a global specialty logistics company that designs world-class logistics and supply chain programs in complete alignment with our customers' business goals. Pharmaceutical companies rely on us because they value the peace of mind that comes with our unsurpassed knowledge, global reach and flawless supply chain execution. Each trusted partnership we form with a customer is deeply rooted in our shared vision of improving global health. With 2,000+ associates in more than 140 offices across the globe, we offer solutions that instill confidence in the on-time, on-temperature delivery of critical products. When trust is absolutely essential, there's only one choice: World Courier.
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