Exhibitors

US United States
Stand No: 14.0C60
Adare is a global specialty pharmaceutical company inspired to create new possibilities for patients whose treatment needs are not fully addressed by current medications. With a growing pipeline, focused R&D efforts, and global manufacturing capabilities, Adare is actively exploring value creation through development and expansion across therapeutic areas. Adare has a proven track record from concept through commercialization that can help you overcome formulation challenges and add valuable IP to your current and future products. Formulation challenges? Experience a partnership focused on the needs of patients and your company's goals, contact us at [email protected]
Location:
IT Italy
Stand No: 3C20
Alfasigma can satisfy all the requirements of the customers because of its ability to manufacture almost the whole pharmaceutical forms even in large or small volumes. Our potential to produce has been brought to the highest level due to the enlargment and the revamping of the plant and the adoption of cutting edge technologies. Alfasigma has worked for 50 years in fields of research, production and selling of pharmaceutical products all over the world. We obtain the know-how to guarantee to customers the greatest quality level in production and all the activities to support new product development.
Location:
CH Switzerland
Stand No: 9B51
Alpex Pharma is a drug delivery business focused on the development and commercial manufacture of effervescent and propriety rapidly dissolving (fast melt) pharmaceutical and nutraceutical products. Our predominant focus is the development of solid dosage forms to deliver drugs directly into the oral cavity in order to potentially improve both the bioavailablity of the drug as well as patient compliance and convenience to it. Alpex Pharma has 28 years of cGMP manufacturing experience and formulation development. Alpex Pharma was established in 1985 as Aesculapius Pharma SA, managed for 12 years by Elan Corporation as Elan Pharma SA. Currently Alpex Pharma employs around 100 people, is conveniently located in Mezzovico, Switzerland, approximately 15 kilometers north of Lugano and 75 Kilometers from Milan.
Location:
DE Germany
Stand No: 5G60
QUALITY, SERVICE AND INNOVATION – THAT'S OUR GUARANTEE TO YOU! We focus on quality "Made in Germany". To guarantee this standard at all times, we carry out our production following GMP guidelines, having been awarded HACCP, BIO and Kosher certificates in addition. Likewise, in the area of quality control, we work according to these regulations so that we can guarantee to meet your requirements and our own for products of the highest quality. The professional expertise of our employees and the high technical standards of our equipment allow us to continually develop the performance potential of Anklam extracts. As an up-and-coming company, we are committed to advancement, just as we are to sustainability. Therefore, we have a strong focus on modern processes and production facilities and the expertise of our experienced employees. On the other hand, we also focus greatly on timeless values such as honesty, fairness, and dependability. Performance,...
Location:
Sub-event: CPWW18
Zone: API
IT Italy
Stand No: 12B14
New
BSP Pharmaceuticals S.p.A. is a Contract Development Manufacturing Organization focused on development, clinical and commercial production and fully dedicated to anticancer products, without any potency limitation. The facility is designed to handle conventional small molecules and ADCs (from Conjugation to fill finish) and very much focused on other innovative therapies. Our services can cover a wide range of manufacturing scales, from the early development up to the commercial, applying the most advanced and safe technologies, in compliance with the highest quality product delivery. The plant is a high containment manufacturing facility designed to achieve an Occupational Exposure Limit (OEL): <10 nanograms/m3. BSP has a manufacturing plant located close to Rome, in Latina Scalo (LT), Italy and a commercial branch in Princeton, NJ (USA). Our production area includes six sterile manufacturing suites (approximately 1850 ft² freeze drying surface in total); an oral department, for solid formulation (tablets, Capsules, Liquid filled hard...
Location:
Sub-event: BIO18
DE Germany
Stand No: 10F73
ChemCon is a contract development and manufacturing organization (CDMO) specialized in transferring drug-substance projects from R&D into fully cGMP-compliant manufacturing processes. Customers worldwide use our services to source APIs for clinical trials and/or commercial applications (i.e., orphan diseases, oncology, or emergency care), excipients, provocation substances, dietary trace elements, diagnostics, delivery agents, or reference standards. Our FDA-inspected facilities are optimized for the production of small to medium quantities. With multidisciplinary expertise we can meet your individual demands for small-molecule organic APIs, inorganic compounds, polymers, and highly potent or controlled substances – all in full cGMP quality up to injection grade. Comprehensive in-house analytics, stability studies, documentation, and regulatory support complete our services. ChemCon looks back on an outstanding inspection history both by the FDA and European health authorities.
Location:
IN India
Stand No: 3B92
Dorizoe Lifesciences Ltd is a purely Contract Research & Finished Product Development Organization based in India, working for Pharmaceutical Companies operating in Regulated Markets. We have strong capability in Finished Product Development of Parentral, Injectable (Lyophilized to Aqueous in Cytotoxic and Non Cytotoxic space) & Semi-Solids Like Creams, ointments & Gel in different delivery systems including Ampoules, Vials, PFS, PVC and Non - PVC bags and so on. At Dorizoe, we have very strong capability of developing injectables in cytotoxic to non cytotoxic space in lyophilized to aqueous form. After developing the product, we can also assist you for contract manufacturing by transferring the technology to your preferred CMO or at our recommended / preferred CMO partners. Apart from contract development, we also provide the Customized Services of Formulation and Development, Analytical Service, Quality Assurance, Regulatory Services and other Pharmaceutical Support Services. Currently we are working with the top pharmaceutical...
Location:
IN India
Stand No: 8J12
Enaltec was established in 2006 with the specific objective to develop and produce niche and technology driven API at competitive prices through its WHO GMP and US FDA approved sites and supply across the world. Enaltec has further strengthen its foothold in generic formulation development through its R&D site Enaltec Pharma Research, having capacity to develop wide range of dosage forms ranging from Solid oral, liquid oral, Derma, Injectable, Potent molecule (Oncology and Hormones), Undertake cGMP analytical method validation and registration ICH stability studies at Enaltec Formulation Labs. ENALTEC= (API R&D + API Manufacturing) + (Formulation R&D [FFS/Turnkey])
Location:
Sub-event: CPWW18
Zone: API
FR France
Stand No: 1G20
FAMAR is a leading European Contract Development and Manufacturing Organization (CDMO) providing a wide range of development and manufacturing services to the Health Care industry. Building on more than 65 years of experience in the Pharmaceutical and Health & Beauty industry, it has established itself as a premier services provider in the Worldwide market. With a network of 12 production sites, 4 Development units, 2 distribution centres, in Europe and North America. Famar offers: • Pharmaceutical Production • Health & Beauty Production • Packaging & QC Testing • Logistics services • Product Development Services via its Technical Development group While each of FAMAR's Business Activities operates as an independent entity, our business culture is based on information sharing and the development of cross-functional synergies, leveraging all of FAMAR's assets to serve our customers with integrated solutions. FAMAR has enjoyed a substantial growth over the last years, gaining a leading position...
Location:
FR France
Stand No: 3D52
galien+ is a new CDMO with 3 sites, located in Burgundy, France @ Auxerre Site is offering a wide range of manufacturing capabilities, with a strong focus on solid doses, powder sachet filling and a dedicated high potent drugs facility. @Nevers, Site is specialized in LYOC - Lyophilized freeze dried tablets (ODT). @ Sens, Site is offering capacities in Blister Packaging, QC, Stability Studies, and a wide range of pharmaceutical services from Analytical Development & validation to Graphic Art services, Scientific and Regulatory services.
Location:
GfM is your reliable partner to micronise and refine your APIs, HAPIs, cytostatics, anti-cancer, hormons and many more products. As contract manufacturer for over 30 years, we are specialists in micronisation, sterile micronisation and milling, for sterilization, cryogenic milling, blending and fractionated sieving. We offer our lab services for PSD (particle size distribution) measurements, PSD method development, transfer and validation. Throughout the world, our customers have come to appreciate our flexibility and expertise while maintaining GMP complying quality and safety standards.
Location:
IN India
Stand No: 12H41
Gracure is a fully integrated pharmaceutical formulation company with in-house R&D, manufacturing and regulatory compliance capabilities. We engage in the research, development, manufacturing, sourcing, marketing, and distribution of high-quality pharmaceutical products. The manufacturing facility have capability to manufacture tablets, capsules, dry syrups, ointments & liquid orals, and is built according to International regulatory guidelines and is approved by EU-GMP, TGA Australia (clearance), UKRAINE GMP and other regulatory agencies like Ethiopia, Uganda, Kenya, Nigeria, Ivory Coast, Ghana and many others.
Location:
GR Greece
Stand No: 14.0F70
HELP S.A. is an EU - GMP pharmaceutical manufacturer with multi product expertise. We provide flexibility and adaptability in Manufacturing. Reengineering is our philosophy. We offer services on Formulation & Analytical Development, Technology Transfer, Contract Manufacturing. More than 45 years of experience in more than 40 countries Worldwide.
Location:
ES Spain
Stand No: 14.1J10
Laboratorios Salvat, privately owned and fully integrated Spanish pharmaceutical company headquartered in Barcelona with US subsidiary in Miami. Salvat: DEVELOPS, MANUFACTURES AND MARKETS high-quality branded pharmaceuticals, both prescription and over-the- counter drugs, in the field of Ear-Nose & Throat, Gastroenterology, Ophthalmology and Consumer Healthcare. Based on its strong commercial capabilities and extensive network of partners around the globe, Salvat has set its goal on the expansion of the company by entering into new territories, adding new products to its portfolio and establishing fruitful, long-term relationships with the international pharmaceutical community. We offer: * LICENSING-OUT our products * Services: CONTRACT MANUFACTURING and CONTRACT DEVELOPMENT We are interested in: * LICENSING-IN finished products for Spain and Portugal
Location:
US United States
Stand No: 3A60
Lifecore has 25 years of aseptic filling experience, focused on viscous and difficult to fill solutions. "Lifecore's" expertise grew from supplying sodium hyaluronate (hyaluronic acid) as an API to its partners and then supplying them with formulation, aseptic filling, and packaging services. Lifecore also does upstream manufacturing for its partners. Lifecore offers the services you expect from a CDMO: Development, Formulation and Process Development, Analytical Method Development, Stability Testing, Technology Transfer, Equipment Design and Procurement, Pilot Batch Sizes for Syringe and Vial Configurations, Quality Systems Experience in Pharmaceutical and Medical Device Regulations, Regulatory Support Clinical and Commercial Manufacturing, Formulation, Sterile Filtration of Highly Viscous Solutions, Aseptic Filling into Syringes or Vials, Secondary Sterilization, Final Packaging, Global Supply Chain Management, Large, Efficient Batch Sizes.
Location:
PL Poland
Stand No: 6C10
Midas Pharma Polska located in Warsaw offers its complex services to the pharmaceutical industry in Poland and Central & Eastern Europe. Based on our global connections we want to become a partner of first choice in the field of active ingredients, dossiers, international licensing, finished forms and regulatory support.
Location:
Sub-event: CPWW18
Zone: API
GR Greece
Stand No: 9F41
PharOS is a privately owned company located in Greece and is considered among the fastest growing Pharmaceutical Development companies in Europe. PharOS is providing a diversified range of own and co-developed pharmaceutical products, including Generics, Fixed Dose Combinations, OTCs and other value added products. With a global portfolio of more than 67 products (27 already launched) and over 6,500 Marketing Authorizations worldwide, we aim to improve the quality of life of patients in more than 85 countries. In addition, PharOS is providing value added services in the field of Product Development, Regulatory Affairs and Business Development Consulting.
Location:
BE Belgium
Stand No: 3H104
Quality Assistance SA is a leading European Contract Research Organisation providing the pharmaceutical industry with all the analytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products. Founded in 1982, the company holds a unique position on the market with 170 highly qualified professionals and all of its laboratories on one site: Bioanalysis (PK/TK/Immuno), bioassays, biochemistry, chromatography, Elemental Impurities, Mass Spectrometry, microbiology, molecular biology, protein characterisation. Quality Assistance is an expert for the development of Biologics (monoclonal antibodies, ADCs, proteins), New Chemical Entities (e.g. peptides, oligonucleotides), Nanomedicine products, Vaccines, Advanced Therapy Medicinal Products (Cell therapy, gene therapy). The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant. Quality Assistance assists its clients from candidate selection, through non-clinical and clinical studies, to marketing authorisation, using state-of-the-art, product-dedicated expertise in analytical sciences. For each customer and each project, Quality Assistance designs customised solutions, define...
Location:
IN India
Stand No: 3H94
Shiva Analyticals ( India) Private Limited is one of the foremost analytical testing labs in India, providing solutions across diverse industries; Pharmaceuticals, Food & Beverages, Minerals & Ores, Fuels & Oil, Industrial Hygiene and Material testing. Our portfolio of services includes providing detailed analytical solutions and testing using state-of-the-art instrumentation and an experienced team of scientists. Our 40,000 sq feet, state-of-the-art laboratory is a fully equipped analytical testing laboratory in Bangalore to test and analyse as per standard, customer- supplied and in-house validated methods. Founded in 1997, Shiva Analyticals has been providing expert solutions to many companies in India and abroad.
Location:
GB United Kingdom
Stand No: 1G74
Source Bioscience is a leading independent, MHRA approved (cGMP) CRO that specialises in chemistry, manufacturing and control (CMC) laboratory services for all phases of drug development. Supporting the pharmaceutical research and development process from preclinical enabling studies, through the clinical research phases and batch release testing into the market place.
Location:
GB United Kingdom
Stand No: 7F40
Sterling Pharma Solutions (SPS) is a leading API CDMO. From US FDA, MHRA and PMDA approved facilities; SPS can handle the most hazardous chemistries at a range of scales. We are passionate about providing a customer focused and service driven approach to offer flexible and tailored solutions to our clients.
Location:
Sub-event: CPWW18
Zone: API
FR France
Stand No: 3F111
Wyjolab SA is an advanced GMP-compliant pharmaceutical laboratory that works with leading healthcare companies to develop and manufacture pharmaceuticals and nutritional products. Wyjolab's state-of-the-art facilities offer customers a wide range of dosage forms (liquids, semi-liquids, powders, extruded polymer, etc.) and many packaging solutions including stick-packs. A strict quality control process guarantees quality from raw materials to finished product. Wyjolab is equipped to conduct constant tests throughout the development process or in ongoing test protocols. With nearly 30 years of experience in product development, Wyjolab also has deep expertise in galenic and analytical services, as well as suspension and oral applicator technologies.
Location:
IT Italy
Stand No: 10F30
Zach System is located in France and belongs to the Group of Zambon. The site has an excellent track record with Authorities (FDA, PMDA, ANSM, etc…). We manufacture API, regulated intermediates, RSM and High Purity Low Endotoxins Excipîents in exclusivity from few kg to tens of tons per year. Our R&D team is constituted of 20 people. We can scale-up processes under GMP using our Kilolab, pilot plant (5m3) and later our industrial workshops. We can handle APIs having an OEL above 1 µg / m3 (OEB 4). One of the characteristic of Zach is its capability to manage many different type of chemical reactions like Hydride Reduction, Lithiation, Cryogenic Reaction, Suzuki & Heck coupling, Ozonolysis (in countinuous at laboratory scale), Grignard, Hydrogenation at different scales (400L, 1000L (5 bar), 2*4000L (12 bar)) and handle dangerous reagents like LAH, DMS, DES, Acetylene, KCN, NaCN, Li in liq. Ammonia, propylene Oxide,...
Location:
Sub-event: CPWW18
Zone: API