Take advantage of our 60 years of global pharmaceutical development and manufacturing services experience. Work hand-in-hand using proven inhalation, transdermal, oral and topical manufacturing expertise from feasibility to market – all while ensuring the highest standards of manufactured product delivery in drug delivery systems.
Aadi Global holds exclusive rights for products of pharmaceutical excipient and API manufacturers for North & South America & the EU. The excipients (superdisintegrants) that can be made available include Sodium Starch Glycollate, Croscarmellose Sodium, Polacrillin Potassium, Calcium carboxymethylcellulose to name a few. We also formulate and distribute Nutraceuticals and some select intermediates like 4-dimethyl amino benzaldehyde, 4-dimethylamino cinnamaldehyde, indicator chemicals for laboratory use.
Direct Salud/Abc Farma, since 1996 is specialized in development, production and distribution on private label of innovative products in the following fields: cosmetics, medical devices, foods supplements. Our product portfolio covers a broad range of therapeutic indications, including Fat reduction · Muscular pain · Wound Care · Anti-aging· Cough & Cold · Skin-Care · Insect Repellent · Foot care · Oral Care · Women's Health · Pediatrics. Gastroenterology. Urology. The range includes unique galenic presentations: transdermal and dermal patches, iontophoretic patches, aromatic patches, vitamin Patches, microneedles patches, oral films, hydrogels, wet wipes. Manufacturing is supported by a certified quality system compliant with ISO regulations 9001, 13485 and compliant with cosmetic GMP guidelines 22716.
Abiogen Pharma S.p.A. Italy offers: licensing out opportunities from its
own product portfolio, Clinical Supply, Contract Development and Manufacturing
A state of the art facility, a strong knowledge and expertise acquired over many years of development and manufacturing of pharmaceuticals, guarantees Clients and Partners high quality standards services.
Accela ChemBio was founded in 2007, as a global leading provider in custom synthesis, process optimization and scale-up production, owned 3 R&D centers, 1 manufacture base, as well as a subsidiary in USA. Our mission is to provide high-quality, innovative products and technical services to our valuable customers. Accela's core business focus in Process R&D and Manufacturing of specialty chemicals and pharmaceutical intermediates.
Accutest is a global independent and internationally accredited Contract Research Organization (CRO) founded in 1998. Accutest offers services to innovator and generics companies around the world and is the market leader amongst independent CROs with highest quality standards and quick turnaround times. Headquartered in Navi Mumbai, India offering comprehensive drug development services in 3 verticals: 1. Bioavailability /Bioequivalence: ACCUTEST is the undisputed leader with an experience of conducting more than 2500 BA/ BE studies for pharmaceutical companies across the world including USA, Europe, Brazil, China, India and more. Today, the company is one of the largest independent CRO in India with the leading market share. 2. Clinical Development Services: Clinical Trials are integral part of drug development. Accutest runs end-to-end services for Phase II to IV clinical trials on small molecules, large molecules and medical devices with fully ICH GCP, complied operations. Accutest is one of the few CRO's providing end-to-end services (protocol writing to CSR submissions) along with stand-alone customized services like clinical data management, medical writing or biostatistics. 3. Services for Biologics and Biosimilars: Accutest Biologics is a state-of-the-art, GLP practicing CRO offering analytical development services for discovery and development of biologics at pharmaceutical and biotechnology industries worldwide. We provide a one-stop solution for analytical services of biologics from early stage characterization to the late stage clinical evaluation of biologics. We can also provide a comprehensive comparative package for demonstrating the comparability of a biosimilar product with that of the marketed innovator product on the basis of both, the physico-chemical and biological characteristics before the preclinical stages and the pre-clinical and clinical comparability post the process development stages. ACCUTEST is ‘One-stop-shop' for end-to-end product development and clinical research. The company has built an unmatched platform to tap the global BA/BE opportunities with GCP and GLP compliant facilities globally. Global accreditation provide the stamp of approval for their quality systems. Accutest has 100+ consistent track records of successful inspections from global regulatory bodies like USFDA, WHO, EMA, DCGI, ANVISA, ISP-Chile, MCC, MOH-Turkey, MOH-UAE, NPCB, Thai-FDA & many more.
is a global specialty pharmaceutical company inspired to create new
possibilities for patients whose treatment needs are not fully addressed by
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]
Our core activity is preparation of DMF / dossiers / CTD / COS / GMP / eCTD. We provide comprehensive solutions for preparation, filling and registration and updates of drug master files (DMF) for API and registration dossiers for formulations. We are an expert in CTD / ACTD dossiers for formulations. We have expertise and experience in preparation, filling and successful registration of COS or DMF for APIs, excipients and packaging materials. We also undertake bioequivalence/toxicity and Phase II III and IV clinical study projects. We also undertake technology transfer projects for finished formulations and APIs.
The Aenova Group is one of the leading contract manufacturers of pharmaceuticals, medical devices, veterinary medicinal products, dietary supplements, cosmetics and nutricosmetics. The group's portfolio of services covers the entire value chain for the development and production of finished dosage forms and product groups in the field of medicines and dietary supplements.
We offer our customers a competent service that covers the galenical and analytical development of products, the optimization of formulation concepts, manufacturing and packaging, right up to support for the certification process. Thereby we are always looking for ways to increase efficiency when it comes to material procurement, production, packaging, logistics, and distribution. We offer our customers tailored solutions for almost every dosage form including Solids, Semi-solids and Liquids. Apart from conventional manufacturing, we offer specialized capacities for aqueous and organic granulation, aqueous and organic coating of pellets and tablets, aseptic manufacturing and Lyophilization. For the handling of a wide range of high potent and cytotoxic APIs, we employ Isolator technology and personal protective equipment. Dedicated facilities are used for manufacturing Beta Lactam oral and sterile dosage forms.
The Aenova Group's high standards of quality, innovative technologies and clear vision for the future have enabled it to become European market leader in the business-to-business field.
The company, which has its headquarters near Munich, operates 20 sites in seven countries throughout the world. All sites are equipped with state-of-the-art technologies and hold all relevant manufacturing licenses and certificates. More than 4000 employees contribute to the group's success.
Aesica is a leading pharmaceutical contract development and manufacturing organisation (CDMO) for both APIs and finished dose forms.
Our full service, end-to-end pharmaceutical development and manufacturing solution comprises capabilities in formulation development for API and finished dose, manufacturing at all scales and packaging services.
We have state-of-the-art facilities and approximately 1300 colleagues at five development and manufacturing sites in the UK, Germany and Italy, as well as an international office in Shanghai and our Head Office in north London, UK.
Our offering is underpinned by our focus on quality, reliability and service, we are aware that customers want more than a supplier, which is why we work in partnership to provide a flexible, efficient and dependable service.
As part of the Consort Medical group, our offering has expanded to include end-to-end capabilities in the design, industrialisation and manufacture of medical delivery devices, further simplifying the supply chain and increasing control for our customers.
AGERON is an international consulting company. We have offices in Poland, Spain and Turkey as well as worldwide network of partners, which allows us to offer global services at the same time optimizing time and costs connected with international scope of projects. From research and analysis, through formulating strategies and recommendations to implementing solutions and evaluation of their efficiency – AGERON offers its clients experience on each step of consulting process. Thanks to that when we start to carry out research or create strategy, we are aware of reality of implementing conclusions later on. When we organize international campaigns or work on schedule for implementing strategy – we understand and take into account strategic assumptions behind specific actions.
Ahn-Gook Pharmaceutical Co., Ltd. is a leading pharmaceutical company in Korea, we're especially strong to Repiratory system and Cardiovascular disease.
Our product, Synatura Syrup is a new drug and No. 1 of antitussive products in Korea, we're already under registration over the 10 countries.
We are accululating core technology to develop new world-class medicine and fostering key manpower that can develop and market our new products.
AIRPHARM is a logistics organization supported by over 25 years of experience in the industry and constantly growing. Our recognized services in transportation, warehousing, customs clearance, cargo handling and logistics consulting on a national and international scale are highly specialized in chemical and pharmaceutical products, without leaving other sectors unattended.
AlbyPharma, formerly known as Suir Pharma Ireland, is a well-established contract manufacturer with 40 years of experience supplying Europe and US market. It has the first oral FDA-Approved Beta-Lactam facility in Europe, Solid Dosage Form facility and Softgel manufacturing capability. All that backed with in-house R&D, Microlab and analytical services.
AAI Pharma Services Corp. and Cambridge Major Laboratories, Inc. have joined to form Alcami, a world class supplier of comprehensive pharmaceutical development and manufacturing services. With seven sites across the globe, our combined capabilities include API development and manufacturing, solid state chemistry, formulation development, analytical development and testing services, clinical and commercial finished dosage form manufacturing (oral solid dose and parenteral), packaging, and stability services.
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.
AllyChem Co Ltd is a fine chemical manufacturing company located in Dalian Economy & Technology Development Zone that specializes in the industrial synthesis of advanced chiral chemicals, diboron esters and multi-functional boronic acids/esters.
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.
· Altex, AINIA´s CO2 Industrial Plant, provides with access to supercritical CO2 processing services, especially extraction and purification processes from First Industrial Trials up to Toll Manufacturing. · Production processes, e.g. APIs extraction and non-desired compounds removal, are customized to achieve the highest performance and flexibility. · Certified CO2 processes: GMP & BIO/ORGANIC.
Altova Healthcare group has its manufacturing setup Blossom Pharmaceuticals at Goa, manufacturing: Non-Sterile Creams, Ointments, Lotions, Gels, Ear drops, Solutions and provides Product Development Services since 1995. Backed by extensive manufacturing, marketing experience & widespread distribution network, Altova Healthcare is one of the most innovative and dynamic companies in India. The facility is WHO-GMP(India) certified and complies with US-FDA, NAFDAC and ISO 9001:2015. Our facility is registered with Srilanka and Ivory-Coast MOH.
Solutions Industry Ltd (PSI) a member of Ambah Group is the
leading sterile injectable manufacturer in Middle East and Africa.
Our manufacturing facilities in Saudi Arabia are GMP certified and equipped with the latest production technologies with over 40 years of proven reliable experience worldwide in contract manufacturing of parenteral solutions in plastic and glass bottles, plastic bags, as well as plastic ampoules.
Recently, Ambah/PSI has developed the first Ibuprofen intravenous (IV) infusion in the world (400mg/100ml). Successfully registered as Ambaprofen and Ambafen (Ibuprofen 400mg/100ml IV Infusion) through the health authorities in Germany, Spain, and Saudi Arabia, its patent has been granted by the European Patent Office (EPO patent no: 2636406) and United States Patent and Trademark Office (uspto Patent No: US 9351926 B2) for its dosage form with the approval of the European Medicines Agency (EMA).
Albany Molecular Research Inc. (AMRI) is a global contract research and manufacturing organization that has been working with the Life Sciences industry to improve patient outcomes and the quality of life for more twenty-five years. With locations in North America, Europe and Asia, our key business segments include Discovery and Development Solutions (DDS), Active Pharmaceutical Ingredients (API), and Drug Product Manufacturing (DPM). Our DDS segment provides comprehensive services from hit identification to IND, including expertise with diverse chemistry, library design and synthesis, in vitro biology and pharmacology, drug metabolism and pharmacokinetics, as well as natural products. API supports the chemical development and cGMP manufacture of complex API, including potent, controlled substances, biologics, peptides, steroids, hormones, cytotoxic compounds and sterile API. DPM supports development through commercial scale production of complex liquid-filled and lyophilized parenterals, sterile suspensions and ophthalmic formulations.
ANFARM SA, a dynamic manufacturer of quality generics since 1967,
promotes its own products worldwide and acts as a third party
manufacturer for multinational companies.
- Lyophilized & Sterile products
- Cephalosporins & Carbapenems
- Non-Sterile Products
Angelini Pharma has a cGMP facility, inspected by US FDA since 1979, and by all international regulatory aothorities. Speciaized in Custom synthesis of API's and Advanced Intermediated, equipped with a Class C (10,000) kilo lab and four production units.
Angelini Fine Chemicals Plants is specialized in Costum's Synthesis of API's and Advanced Intermediates. It has 140.000 Lt gasslined and Stainless steel Reactor Capacity and a Pilot plant with 250 -800 Lt reactor capacity. Multipurpose technology base, full analytical services and support, blending and sieving. Flow Reactors allowing new syntheses heretofore not possible, increase yields, product quality, scalability and efficiency of Chemical processing, reducing the performance variability and costs.
Leader in the wellness industry, a point of reference in the field of health protection, Angelini is the natural choice for daily wellbeing.
Angelini manufactures, markets and distributes products for personal health and wellbeing.
Angelini is an "integrated company" with extensive research, development, manufacture and marketing of active ingredients, and equivalent branded drugs, medical products and dietary supplements. At the international level, Angelini is concentrated in the areas of analgesia and inflammation, neuropsychiatry, flu, diseases of the oral cavity, gynecology, personal hygiene and disinfection.
The most well-known international brands are Trittico, Tantum and Aulin. Locally, Angelini is focused on specific areas thanks to the strength of its brands.
In Italy, Angelini is one of the first pharmaceutical companies and specializes mainly in analgesia and inflammation, neuropsychiatry, influenza and diseases of the oral cavity, gynecology and disinfection.
It is also present with a line of generic drugs (Angenerico) that includes about 60 molecules.
Anhui HeGeng Biotech Engineering Co., LTD. a bio-based raw material manufacturer of R&D, derivative application, production and sales.We concentrated on monosaccharides, nucleoside activation,glycosylated modification, polymerization for high purity grade products and excipients and downstream bio-pharmaceutical, bio-fermentation components technical developments and specialized applications.L-Arabinose, D-?+?-Galactose, L-rhamnose monohydrate, D-Glucuronic acid?D-Glucaric acid. Nucleotide activated monosaccharide, Carbohydrates enzymatic synthesis of the key substrate.
Anlit develops and produces high-quality dietary supplements for the whole family. With product R&D innovation as its hallmark, the company has a complete portfolio of shelf-ready products. Anlit's mission is to make nutritional supplements friendly, easy and comfortable for everyone. Anlit products are consumed daily (and happily) by adults and children in more than 25 countries around the world, including the United States, Europe, Russia, Southeast Asia and South Africa. The company has built its reputation on science-backed innovation, quality and responsiveness to customer requirements. Studies show that kids , but not only, are more likely to take food supplements that are appealing to taste, touch, smell and sight. Anlit's products are designed to address child and adult preferences with its proprietary delivery systems: pectin-based gummies bears and VitaBites chewables. Anlit is continuously innovating and perfecting its products, formulations, technologies and delivery systems, setting industry benchmarks and introducing progressive products to the market.
APC accelerates product development through the combination of innovative technologies ranging from process modelling, automated lab reactors and process analytical technology with in-house developed capabilities in continuous processing, process control and advanced analytics. APC delivers development solutions, across all clinical phases and addresses post-market challenges, irrespective of the therapeutic area.
APISystems Sp. z o. o. is a company offering the latest solutions in the field of Industrial Informatics, mechanical engineering and production sites. We form a group of experts dealing with the complex investment implementation. We offer high quality services. Every day we support our clients with knowledge and experience. We treat our clients as partners for long-term cooperation. Over 11 years of operation, we have completed over 300 projects in the field of Industrial Informatics and production automation. Since 2011, we have been a Wonderware Certified System Integrator. We run projects in Polish, English and German. MISSION: Achieve the leading position in Europe as the Wonderware Integrator System. POLICY:Provide the highest quality offer for the industry.Maintain good relations with partners. Get new knowledge and competences every day. Be ready for new challenges, join new markets and industries. Run the company so that employees eagerly come to work.
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€.
Aptiekas Produkcija is a leading Latvian manufacturer of a wide range of quality finished food supplement/ Nutraceutical products for a variety of market segments. Our competitive advantage with regards to the finished products is an uncompromised quality yet at highly effective price and a very stimulating policy for distributors. Aptiekas Produkcija is a leading Latvian manufacturer of a wide range of quality finished food supplement/ Nutraceutical products for a variety of market segments. Our competitive advantage with regards to the finished products is an uncompromised quality yet at highly effective price and a very stimulating policy for distributors.
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.
Established in 1972, Arnet Pharmaceutical has researched, manufactured and marketed natural products worldwide. Arnet Pharmaceutical is internationally recognized contract manufacturer, known for its quality and service. Our facility includes offices, laboratory, manufacturing and warehouse areas and includes separate rooms for our production machinery. Arnet's extensive line of products includes a complete range of vitamins, minerals amino acids and herbal supplements. Arnet also has the capability to do: Tablets, Hard Capsules, Liquid Capsules,Powders and Chewable. WHY ARNET PHARMACEUTICAL · Our, FDA (Food and Drug Administration) registered facility has established Standard Operating Procedures (S.O.Ps) to ensure compliance for potency, disintegration, dissolution and microbiology every lot · All formulas are manufactured in compliance to establish FDA Good Manufacturing Practices (21 CFR 111). · We have extensive experience in developing unique custom formulations. We provide only the highest quality products from the finest ingredients. · We offer flexible options for packaging: bulk packaging, bottled packaging (with or without individual box), and special packaging (in blisters, packets, pouches or sachets). · State-of- the-art 85,000 sq. ft. facility, all air-conditioned site under a controlled environment. · GMP Certified: o Kingdom of Saudi Arabia MOH o NSF (National Sanitation Foundation) o NHPD (Health Canada) o SGS · Halal and Kosher Certification. · On Site Chemistry & Microbiology Laboratory. · In-house art department and labeling regulatory compliance that develop labels and package designs. · All specifications and methods of analysis are developed under the United States Pharmacopeia (USP) guidelines. · Stability Program (Accelerated & Real Time). · Assistance to our clients with their product registration process in their country, if required by the local health authorities.
We specialize in the transport of pharmaceuticals under conditions of controlled temperature. We are authorized to carry all classes of drugs. We comply with good distribution practice of medical products and guidelines contained in the Official Journal of the European Union. We use our knowledge and experience to provide the highest level of service. Our freight forwarders will advise you on the most beneficial and safest form of transportation of your goods. Specially trained drivers ensure a constant temperature during transport and the protection of pharmaceutical products against external contamination. Our cars are equipped with temperature monitoring, which allows you to verify it in real time.
ARTESAN is a premium partner for the pharmaceuticals industry. As a contract manufacturer for solids, lozenges, liquids and sterile syringes, we focus on quality, individual customer service and cost-effective solutions. We continuously invest in the development of new formulations and recipes, and state-of-the-art packaging technologies.
ASM is a leading company in developing, mixing and filling high quality pharmaceutical and cosmetic products in liquid and semi-liquid forms. This includes Standard-Aerosols, Bag-on-valve Systems, Sticks, Airless-systems, Bottles etc. depending on customer's requirements. ASM is a proactive and innovative partner and provides complementary services such as project management. With its broad know-how, ASM offer the optimal support and also collaborates with external partners like consultants, suppliers, universities, etc. ASM has the ISO 9001 : 2015, ISO 13485 : 2016 and ISO 22716 : 2007 certificates as well as GMP and FDA certification.
Asmontec provides complete solutions for Clean Room Engineering, working with excellence, ethics and transparency through all stages of the process: project development, production, construction and maintenance. With over 22 years' experience in the field, we establish service credibility and products' quality as our leading features, in order to offer the best solutions to our costumers. Keeping quality as main priority, Asmontec plans and develops products according to each client specific needs, ensuring its ideal implementation. We are specialized in the fabrication and installation of doors, pass through, panels, glazing line and acessories for clean rooms. Complying with GMP (Good Manufacturing Practices), ANVISA (Health Surveillance National Agency), FDA (Food and Drug Administration) and SBCC (Brazilian Contamination Control Society) requirements and acceptance criteria, our products are specified according to a previous study of resistance and wear to meet the client's needs, being developed with smooth surface and no edges, avoiding particles' release and contamination.
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.
· Regulatory and Scientific Strategy during Development
· Medical and Scientific Writing
· Global Submissions
· eSubmission and RIM
· Life-Cycle Outsourcing
· Promoting the marketing registration of Medical Devices: Classification strategy, CE Marking and compilation of technical file.
Aurisco is an innovative company dedicated to developing and manufacturing pharmaceutical chemicals serving pharmaceutical companies worldwide. With 2 manufacturing sites for chemistry synthesis & fermentation, all of which are operated according to cGMP standards, Aurisco offers Active Pharmaceutical ingredients (APIs especially in segments of Steroids, Oncology, Anti-Virus and etc.) and drug intermediates as well as contract developing and manufacturing of pharmaceutical chemicals from kilos to tons.
With over 100 years of experience in dairy and more than 75 years of experience in the development and production of infant formula, Ausnutria manufactures tailor made infant nutrition for customers around the world. In addition, Ausnutria supports the growth and development of babies and children by offering premium infant formula brands Kabrita and Neolac Organic. Ausnutria works together with customers to develop and produce tailor made infant formula. Ausnutria owns five production sites in the Netherlands, in which the production of infant- and toddler nutrition is fully integrated. With these factories, Ausnutria controls the entire production chain from fresh cow's milk to infant formula. Ausnutria offers full support to the customer, ranging from infant formula production only, to full support in product development, R&D and marketing. The Ausnutria infant formula factories have enough production capacity for large international orders. In further consultation, the possibilities for smaller orders can be discussed.
Avanti Polar Lipids Inc is the world leader for lipids of unparalleled purity. The company manufactures products for the Research Chemist and cGMP lipids for Pharmaceutical Production. These include phospholipids, sphingolipids, detergents, sterols, polymers, bioactive lipids, chelators plus new Fluorescent and Deuterated lipids. Recent developments include unique Detergents, Adjuvants, Glycosylated Sphingolipids and Kdo2 Lipid A - an Endotoxin replacing LPS. Avanti is the licensed manufacturer of mass spectrometry standards to the LIPID MAPS Initiative. Avanti's extensive Lipid Analysis Department handles Identity Testing, Bioanalytical Lipid Assay and cGLP & 21CFR, part 11 Compliant Analysis. Avanti's clients include the Pharmaceutical & Nutraceutical Industries and Lipid Researchers.
Avara offers contract manufacturing of APIs, solid and liquid sterile drug product, and packaging from nine world-class facilities. Led by highly experienced industry veterans, Avara understands clients' individual needs and focuses on providing an exceptional outsourcing experience by delivering on commitments in terms of scope, schedule, compliance and price.
AVEFLOR offers complex services starting from development of new products, their certification, purchase of raw materials and packing materials, to actual production and delivery to the customer. The company is also a holder of a certificate of the due production practices for the production of pharmaceuticals and the production takes place within “clean premises”. AVEFLOR has been producing liquid and powder aerosols since its foundation (1995). In 2007, the company extended its range of technologies by including the production of emulsions and gels in plastic containers and in BOV aerosols.
AXXO is a leading international supplier with a rich product portfolio covering a wide range of therapeutic categories including active pharmaceutical ingredients (API), intermediates, finished dosage forms as well as the latest development in the field of biotech production i. e. monoclonal antibodies (MAB).
Our international operating company would be pleased to offer you our custom-made services from developing, manufacturing and marketing APIs, finished dosage forms or registration dossiers to full health concepts like machinery & equipment for your own manufacturing.
We are present in the EU, in a huge number of the CIS
countries and in various South American and Middle East markets. Our product
portfolio embraces APIs as well as finished formulations. Our dynamic and
highly-motivated team is investigating, developing, producing and distributing
innovative pharmaceutical products. We are offering just-in-time delivery,
customized product parameters as well as registration assistance.
Our expertise consists in the development and
registration of pharmaceutical products with a special emphasis on
Biotechnology, Oncology as well as Generic Drugs.
The headquarter of AZ GROUP locates in National Health Technology Zone of Zhongshan City, Guang Dong Province, P. R. China. It covers an area of 35,000 square meters, with the convenient transportation of one hour from Hong Kong by ferry. As an international and US FDA cGMP approved company, AZ GROUP is a Sino-US joint venture integrates R&D, manufacturing, marketing and customer services, it has been dedicating to the career of human health since its establishment. The product of AZ GROUP includes Pharmaceutical Products, D-Cal Calcium Supplements, Nutraceuticals and Health Food. It has a variety of international advanced manufacturing & testing equipments and refined production technologies. Strict quality management system and the internationalized specifications have been established to ensure the product quality. Some of our products are US FDA approved and exported to the countries including U.S.A, Europe and Canada etc.
Azelis is a leading supplier of active pharmaceutical ingredients (APIs) and excipients for the pharmaceutical, veterinary and health care industries. We are GMP certified by both the MHRA and Bezirksregierung Düsseldorf and have the required authorisations for distribution of psychotropic drugs and for controlled substances. Our dedicated team of more than 65 specialists includes expert pharmaceutical formulators and flavour technologists to support your new product development. Our Applications Laboratories provide full evaluation capability for all topical healthcare applications. Our technical sales support teams, backed by unique sourcing and integrated delivery systems can help to drive up quality, while reducing costs.
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).
B. Braun – Industrial Partnerships provides a broad range of services and manufacturing of pharmaceuticals and medical devices. Based on 175 years of experience, we serve the needs of our customers with customized system solutions and contract manufacturing services from our global development and manufacturing network.
Baxter International Inc. provides a broad portfolio of essential renal and hospital products, including home, acute and in-center dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; biosurgery products and anesthetics; and pharmacy automation, software and services.
Beijing Hope Pharmaceutical Co.,Ltd. (stock
number 836438), founded in 2005 and located at Beijing Economic-technological
Development Area, is a state level high-tech enterprise dedicated to the
development, manufacture and promotion of chemical drugs. According to GMP and
related regulations, together with partners, manufacturing sites have been
built in Shandong, Hebei, Anhui, Zhejiang province which have passed the
domestic GMP qualification and customers' audits of European and North American
Beijing HMT Medical Technology Co., Ltd. (HMT) is a wholly owned subsidiary of Hope specialized in R&D, manufacture, sales of Pharmaceutical Intermediates (PIs) and is oriented towards the global market. Depending on many years' experience in drug R&D and registration, we can provide our client not only the high-quality products, but also comprehensive technical and document support to assist them in solving the problems.
Dr.JCR BIO, leading manufacturer and supplier of Pharma reference standards includes Impurities and metabolites. We have a world class research facility to provide contract research (CRO) and custom synthesis (CMO) includes CRAM's at Hyderabad, India.
Beijing Huikang Boyuan Chemical Tech Co Ltd established in 2005 is a high-tech enterprise and specializes in research and manufacture of new drugs, APIs and pharmaceutical intermediates.
Established in 1978, Biocon Limited, is India's largest, and Asia's leading, biotechnology company with a strategic focus on biopharmaceuticals and research services. It is a fully integrated, innovation-driven biopharma enterprise offering affordable solutions for chronic diseases to patient's worldwide. We develop, manufacture and deliver a rich portfolio of Small Molecules APIs & Formulations and Complex Biologics - both Novels and Biosimilars - including MAbs, rh-insulin& Insulin Analogs. Biocon's robust product portfolio includes the world's first Pichia-based recombinant human Insulin, INSUGEN, Glargine, BASALOG and India's first biologic BioMAb-EGFR; for head and neck cancer. It has now successfully developed its second novel biologic Itolizumab, a 'first in class' anti-CD6 monoclonal antibody, being introduced as Alzumab; for psoriasis in India, in 2013.
Biodue SpA was founded in 1986 by Sion Fulvio Benedetti and develops manufactures and distributes Medical devices, Skin cosmetics and Dietary supplements (in solid and liquid forms). In 2017, Biodue reached a turnover above 36 Million Euros and about 170 employees. The plants and warehouses cover almost 17.000 square meters and all of them are located in an industrial area near Florence. The company has two main core businesses: the Industrial division, focused on contract manufacturing and the Brand division, focused on the commercialization and promotion of the company's own products. Within the Brad division, there are three Brands: Selerbe's portfolio, based on herbal products, promoted to pharmacies; Pharcos' portfolio, including medical devices, food supplements and cosmetics, promoted to dermatologists and Biofta's portfolio, including medical devices and food supplements, promoted to oculists/ophthalmologists. The company commercialize and promote its own products directly in Italy and through JVs in US and Latam; the company has in place agreements with local/regional partners in several geographic areas not covered directly. The company has recently developed and patented in EU and US an innovative technology - RewCap® - applicable to vaginal douche, mono-dose food supplements, drops food supplements and mono-dose medical devices. The company is registered under EC Regulation number 852/2004 and under GMP (Good Manufacturing Practices) certification. The company is also registered with the US Food and Drug Administration (U.S. FDA Registration no.10725095718). From May 2015, BioDue S.p.A. is listed on the Italian stock exchange in the AIM sector. The Company received the ISO 13485 certification for the development, manufacturing and production of medical devices.
extremely modern pharmaceutical plant, which manufactures antibiotics,
sulfonamides, compound feeds, dietary supplements, syrups, ointments and
creams, suppositories and vaginal globules. Our plants have integrated quality
assurance systems such as: GMP, HACCP, ISO 9001:2008. Moreover, one of them has
CE certificate for medical devices according to EN ISO 13485:2012 and AC 2012
and Medical Device Directive 93/42/EEC. Biofaktor performs contractual
production of medicinal products and dietary supplements for various
clients around the world.
We have successfully finished over 200 projects related both to development and manufacturing of the products of various categories.
Biofaktor has a huge possibilities and rich experience in product development, laboratory analysis, drawing up documentations and final production. Our expertise covers all major product groups, namely:
- food supplements,
- medical devices,
- OTC medicines,
- RX medicines,
We are also experienced in additional services:
- formal management of technology transfer,
- process adaptation if required,
- pilot runs,
- stability tests,
- full scale production,
- release analysis,
- tablets (various sizes, shapes, film and sugar coated),
- hard gelatin capsules (sizes: 1, 0, 00),
- granules (incl. coated granules),
- suppositories, vaginal globules,
- non sterile liquids,
- emulsions, balms
- blisters Alu/Alu,
- various containers with different pumps, applicators (incl. Oral and nasal)
sachets for: ointments, gels,
BioFilm has established an excellent reputation for developing and manufacturing thin dissolvable films (TDF) which release active ingredients. A range of actives can be incorporated into the films and the products can be classified as nutritional supplements, cosmetic, dental, medical devices through to medicinal and pharmaceutical. In fact, we produce more products in TDF than any other European manufacturer. BioFilm can offer companies a true partnership which allow us to take innovative concepts right through from initial research to development, manufacture, packaging and final delivery to the retailer. Thus enabling partners to launch innovative products quickly and cost effectively. Contact us today to learn more to discuss potential collaborations.
is a leading Thai pharmaceutical company specialized in the manufacture of a
wide variety of pharmaceutical formulations, including sterile preparations
(small volume liquids and powders), tablets, capsules, powder, liquids,
ointments and creams. Thanks
to our innovations of new generic products and a continuous quality improvement
that allow us to maintain the position of leadership, BIOLAB has become
synonymous with “world class quality”. Our current facilities can support the manufacturing of
niche products, including sterile powder products, lyophilized products and combined hormonal
respect to the contract manufacturing services, we deliver customized services
that respond well to various demands of customers. BIOLAB is
entrusted by renowned Thai and international customers, including Germany,
Japan, Italy, Malaysia, Singapore, Philippines, and Sri Lanka as a contract
manufacturer of their pharmaceutical products. We continue to expand our
presence in global markets and are devoted to satisfying customers with our
quality products and services.
BioVectra is a contract development and manufacturing organization that serves pharmaceutical and biotech companies with full-service cGMP outsourcing solutions for intermediates and active pharmaceutical ingredients (APIs). An innovative and reliable partner with a strong quality history, BioVectra has over 45 years of experience specializing in:
- Microbial Fermentation
- Complex Chemistry
- High-Potency APIs
- Process & Analytical Development
- Drug Development