Eurofins Alphora provides API technology development services for complex niche small molecules, covering pre-clinical to Phase III and commercial manufacturing. Alphora operates FDA-approved facilities totalling 51,000+ ft² including cGMP Kilo Laboratories and cGMP Plant operations, R&D and Analytical laboratories, QC/QA, as well as a separate high potency/cytotoxic facility.
Eurofins Amatsigroup is a leading international Contract Development and Manufacturing Organization (CDMO), headquartered in France. Within Amatsigroup, we provide high-quality, customized and cost-effective drug development solutions, integrated under one roof, to small biotech and major (bio) pharmaceutical customers. Our innovative and flexible approach enables customers to speed up their drug development process, achieving key milestones in a timely manner. The company has three strategic pillars:
- Drug substance process development and manufacturing for biologics,
- Pharmaceutical analysis solutions: fit-for-purpose method developments and validations, stability studies and Quality Control (QC)
- Formulation development and manufacturing of sterile and non-sterile clinical or small commercial batches.
Global BioPharma Product Testing within your reach As the largest international network of harmonized GMP and GLP product testing labs, Eurofins BioPharma Product Testing delivers a true local service experience. Eurofins BioPharma Product Testing offers the most complete range of testing services, harmonized quality systems to more than 800 virtual and large pharmaceutical, biopharmaceutical and medical device companies worldwide. In Our World, Global Is Local Our local presence ensures personal service backed by a unique global breadth of harmonized capabilities that support all functional areas of bio/pharmaceutical drug development and manufacturing, including method development, microbiology, process validation and quality control. With a global capacity of more than 92,000 square meters and facilities located in Australia, Belgium, Canada, Denmark, France, Germany, India, Ireland, Italy, Spain, Sweden, Switzerland, Netherlands, New Zealand, UK and the US, our network of GMP laboratories operates under the same strict quality procedures, LIMS and centralized billing system across 28 locations worldwide. Further, we have teams of scientists placed at more than 44 client facilities throughout Europe and the U.S. through our award-winning Professional Scientific Services (PSS) insourcing program. Experience Our Expertise We offer complete manufacturing control testing services for the pharma and biopharma industries, including all starting material, process intermediates, drug substance, drug product and manufacturing support, as well as broad technical expertise in Biochemistry, Molecular & Cell Biology, Virology, Chemistry and Microbiology. International Presence Means Global Regulatory Compliance Operating under the same strict quality procedures, our laboratories offer a broad range of methodologies under GMP authorization, ISO 17025 accreditation and ISO 9000 certification, and all analysis are performed according to European and British Pharmacopeia (EP), United States Pharmacopeia (USP) and Japanese Pharmacopeia (JP), as well as specific customer methods. Our fundamental philosophy is to help clients efficiently allocate their research and manufacturing expenditures by strategically engaging them to meet their unique outsourcing needs.
Europhartech, a contract manufacturing and development organization, has been recognized by pharmaceutical (human and veterinarian) and food supplements industries, for the adaptability of its services and the mastery of its supply chain. Thanks to high performing equipment, with continuous developments, Europhartech manufactures, in a fullservice approach, solid dosage forms for oral use (princeps, hormones, hospital, unit dose, probiotics, generics and food supplements). Uncoated, film/sugar/coated, flash tablets, hard gelatin capsules, and plant extracts drying with microwave technology. Blisters packaging (PVC, multilayers/alu, alu/alu) pots filling with counting control. Europhartech also offers development services, including production of pilot batches, stabilities studies until the industrial transposition.
Eurpack, Italian leader in the production of primary and secondary packaging for industries in the pharmaceutical, cosmetic, healthcare, and retailers areas. Innovation in design, materials and technical solutions, performed on our R&D department side-by-side with our Customer. Every year we produce 500 million folding boxes, 85% of them dedicated to the pharmaceutical market in a wide range of formats, technical solutions and standards in continuous evolution. The best technologies and our expertise applied on the printing of aluminium for blisters. Printing made in controlled rooms, and on several production line. in continuous, in two plants. The three distinctive key points of Eurpack (flexibility, great production capability and assured quality) are concentrated in the production of leaflets, necessary accessory of the pharmaceutical packaging. Packaging is not only printing, but also innovation and ability to follow the evolution of markets and legislation. For this reason, Eurpack has created a division dedicated to the production of serialized folding boxes, at the avant-garde for security, quality and accuracy. We design and realize displays in high and limited batches. A challenge of productive engineering and communication that, with always-new forms and colours, adds value to the final product and attracts the Csutomer's attention.
EVA Group Limited is health care organization
established on the heritage of 100 years of experience in the pharmaceutical and
personal care fields, and compromises a group of companies including EVA Pharma
and EVA Cosmetics. EVA Pharma is a rapidly growing branded generics
pharmaceutical manufacturer operating in frontier markets with a presence in more than 30 countries globally, EVA Pharma has state-of-the-art facilities which are approved by EMA and other regional authorities and it has a comprehensive portfolio of more than 130 product focusing on
Endocrinology, Hepatitis, Orthopedics, Urology & CNS. EVA Cosmetics is a
leading personal-care manufacturer whose products are considered as an integral
part of consumers' daily lives in more than 20 countries across the globe.
EVER Pharma is an Austrian based fully integrated specialty
pharmaceutical company focused on research, development, production and
commercialization of innovative therapies and value-added formulations. Our
product portfolio and pipeline currently covers the therapeutic areas of
neurology, critical care, anesthesia and oncology. Our finished dosage form
products are developed and manufactured at our EU GMP certified facilities in
Austria and Germany and marketed in more than 70 countries around the world
through affiliated companies and strategic partners.
In addition to our own product portfolio, we offer years of experience and ‘know-how' in providing full service manufacturing for global partners. Covering fill & finish, QC, stability testing and warehousing we provide high quality sterile production of ampoules, vials, syringes and implants. Our extensive specialized service capabilities includes the production of highly complex injectables such as high potency substances, crystal suspensions and oil based formulations.
The company was incorporated on 19.02.1993 to manufacture bulk drugs viz. Omeprazole, Ciprofloxacin, Dichloroflurobenzene, Benzimadizole, etc. The construction activities started in 1994 and the commercial production of the company started in 1996. We are one of the major manufacturers & exporters of Active Pharmaceutical Ingredients and its intermediates in India.
We are an ISO 9001-2008 certified company and our facilities comply to GMP standards and are certified by the Drug Control Authority of the Government of Andhra Pradesh, India. Our products comply to various pharmacopial standards like BP, USP, EP and IP Standards, as desired by the customer, as well as our own in house specifications. If required, we can provide Drug Master Files (DMF) and Common Technical Documents (CTD) for our products. We have also achieved a high degree of purity standards consistently for all our products and our documentation support is extensive as we have been dealing with these products since 1996.
We supply our products to major multinational companies abroad, prominent well established formulation companies in India, Europe, USA, Far East and the Middle East, and also to Latin / Central / South American Countries.
Everlight Chemical Industrial Co. founded in 1972 started to develop prostaglandin APIs in 1992. We achieved sustainable growth by balancing economical, social and environmental responsibility and worker's safety. Our APIs have registered worldwidely, including US, Canada, UK, EU, Japan, China, Russia, India, South America, Egypt, Middle East etc. Our plant is certified by Taiwan FDA, US FDA, EMEA, PMDA, Swedish MPA. To date, our sales are widely distributed over 40 countries in the world.
EverZinc is a global leader in the production of zinc materials with three product lines: fine zinc powders, zinc oxide and zinc powders for batteries. Main Zinc Oxide producer of Europe, EverZinc is also the sole manufacturer of Zinc Oxide as an API. We produce very pure quality material, conform ICH Q7 (GMP certified). Everzinc is the only ZnO producer in Europe with a CEP. EverZinc focus on innovation; we will build our future thanks to the development of new products and services that better serve our customers.In the recent years we have launched successfully an ultrafine zinc oxide (Zano®) for personal care industry but also for new applications in plastics, textile and electronics.
Evonik Industries provides solutions to the pharmaceutical and biopharmaceutical industry for tomorrow's needs in drug development, manufacturing and drug delivery. As a leading speciality chemicals manufacturer, it offers the broadest portfolio of know-how, products and services available in the market: From biotechnology based products to custom intermediates, from excipients for drug formulations to drug delivery technologies, we provide expertise, service and technology that create competitive advantages for our customers. For customers manufacturing APIs and intermediates Evonik is a globally leading supplier of heterogeneous catalysts as well as homogeneous metathesis catalysts which all can be tailored to customer needs.
Ewopharma AG is the innovative partner for the marketing of pharmaceuticals and consumer health products in Central Eastern Europe. With over 50 years' presence in the region, Ewopharma has extensive knowledge of these markets and enjoys a privileged position in the area.Ewopharma represents regional and international pharmaceutical partners as their exclusive licensee and distributor and covers all aspects of market access and commercialisation of ethical pharmaceuticals and consumer health products. The company employs more than 320 highly qualified staff in over 16 countries.Ewopharma has a strategic focus on specialty pharmaceuticals for its hospital business and provides specialists with innovative products for medical conditions with high unmet medical need. Ewopharma medical representatives visit specialists in strategic areas suchs as gastroenterology, allergology, immunology, oncology and neurology. In OTC/Consumer Health Care, Ewopharma focuses on hair loss and hair cosmetics, digestive disorders and products for cough and cold. Further information is available at www.ewopharma.com
Since 1991, Exim started to promote Indian origin Pharmaceutical products and has built a solid reputation as a reliable, transparent and ethical partner. With exceptional sourcing abilities and strong regulatory, logistics backup, we successfully service customers spanning 50 countries. Our strength are API's, Intermediates, Excipients, Custom-Synthesis , Nutraceuticals & Vitamins.
pharmaceutical companies, manufacturers, developers and laboratories
around the world.
Our broad range of services include:
Technical Project Management
Medical Device Development
Technical Due Diligence
Qualified Person Services
Process Analytical Technology (PAT)
Quality by Design Development