We are a global leader with 100 years experience in the research, development and manufacturing of high-grade activated carbon as purification aid in the pharmaceutical and other industries. Our powdered, granular and extruded activated carbons are used for the removal of colors, odors, by-products, traces of catalyst or any other impurities that aren't allowed in the final product. Under the NORIT® brand we produce medicinal products based on activated carbon including contract manufacturing. We meet the most stringent quality requirements that guarantee consistency in performance and purity. Our specialists can support you selecting the best activated carbon for your process in the early drug development phase, scaling up and full production.
Cafosa is the world's leading supplier of innovative and high performing gum bases, chewing gum's main ingredient. Cafosa dedicates its activity to confectionery, nutraceutical and pharmaceutical industry.
To dedicate to the nutraceutical and pharmaceutical industries, since 2014 there is a new business unit, Cafosa Health. Cafosa Health vision is to develop the functional and medicated chewing gum category, as a friendly and efficient way to deliver health and wellness.
About Cafosa, the company was founded in Barcelona in 1979 and belongs to the Mars group of companies, one of the world's largest food companies that produces global brands. Cafosa guarantees a reliable supply and top quality products and services to contribute to our customers' success in the chewing gum market. Our products are manufactured in accordance with the Food Good Manufacturing Practices and raw materials used comply with the most demanding Food Safety regulations. Our facilities, products and management system comply with the most outstanding pharmaceutical requirements. Sourcing from Barcelona and Shanghai, we ship to more than 80 countries worldwide. Cafosa is member of the International Chewing Gum Association (ICGA), Produlce, Leatherhead and AINIA.
With a long history in the distribution of base and specialty ingredients, API's, intermediates and excipients, Caldic is well known in the Health and Personal Care industry. We offer our customers high quality products and support them in the development of new products right from the development stage to production. We take advantage of our worldwide network of companies with our own facilities such as a white room, filling lines, HACCP services combined with a synergistic product portfolio.
Callery, the experts in reagents that enable YOUR chemistry. We are recognized world-wide as the experts in (1) Borane-derivatives for: reduction reactions, free-radical sources, coupling chemistry and chiral reagents, and (2) Non-nucleophilic bases for deprotonation reactions for coupling and elimination (alkali metal alkoxides and alkali metal HMDS salts). Our expertise in handling air- and moisture-sensitive reagents assures the highest quality products are delivered to you on time and on spec. Talk to us about safe-handling training and engineering recommendations - we are happy to support your engineering and manufacturing teams to insure our products are safely fed into your process at the same quality they left our packaging department. From sub-kilo samples to truckload quantities, we can support your demand and make you successful!
Cambridge Isotope Laboratories Inc is the world leader in the manufacture and separation of stable isotopes and stable isotope labeled compounds. CIL offers an array of highly pure compounds that are uniformly or selectively enriched in 13C, 15N, D, 18O or 17O. CIL offers over 15,000 stable-isotope labeled products for use as internal standards and in synthetic applications, including the manufacturing of APIs. CIL maintains one of the only privately held (non-governmental) D2O re-enrichment facilities at our isotope separation facility to further ensure continuous supply of D2O for manufacturing. CIL's capabilities range from milligram to multi-kilogram of deuterated reagents and intermediates. In addition, cGMP suites for manufacturing clinical trial grade materials (CTM) are also available.
Camida is a leading supplier of organic intermediates, organometallics, fine chemicals and infinite other chemical specialities to the pharmaceutical and chemical industries. Products are supplied on a scale from gram to multi-tonne quantities from a variety of sources around the world. This includes intermediates for new chemical entities and pilotscale quantities for clinical trial production through to the bulk supply of raw materials at competitive prices. A technical sourcing department with global contacts and network is available for customers needs.
Established in 1996, Capot Chemical Co Ltd is a custom synthesis manufacturer, headquartered in Hangzhou, P.R.China. As an ISO 9001:2008 certificated company, Capot has a safety management system in place. It produces a wide range of organics, especially fluorine, boronic acids, unnatural amino acids, cross linkers, chiral building blocks, heterocyclic compounds and other active pharmaceutical ingredients. Capot has established a global network of customers from many research centers, pharmaceutical companies and chemical factories.
Capot has experienced experts, excellent manufacturing equipment, and a advanced R&D center. It owns the ability to provide products from a few grams to kilograms, even to tons. And it also provides custom synthesis service, to help its customer with its best efforts.
In capot, we care about the quality and success of our customers' projects as if they were our own. We are committed into providing the reliable quality, competitive prices and superior service to our customers.
Capricorn Life Sciences offers pharmaceutical products with valuable USP's for marketing and distribution and/or in-licensing (medicines as well as Food for Special Medical Purposes (FSMP), food supplements and medical devices) all with clinical backup.
Our product portfolio covers a broad range of therapeutic indications and includes unique galenic presentations such as vapor patches, stickpacks, controlled release tablets, effervescent tablets, nasal sprays, oral sprays and throat sprays.
Efficacy and safety of our products have been proven in clinical trials and/or are supported by approved EFSA claims.
Manufacturing is performed by various European GMP and/or HACCP approved factories, ensuring a guaranteed and constant high quality.
The products can be marketed under our ready brands but we are open to discuss supply under private label as well.
Complete EU regulatory dossiers and full regulatory support are provided.
IMPORTANT: if you are on the intitial page of Capricorn's profile in "Exhibitor List" click the blue button "More Information" if you want to see all our products (below is shown only a small selection)
Capsule Delivery Solutions, part of Lonza Pharma Biotech, is the global leader in capsules and encapsulation technology and designs. Their unique combination of science, engineering, formulation and capsule expertise enables customers to optimize the bioavailability, targeted delivery and overall performance of their products. More information about the Capsugel® product range is available on www.capsugel.com.
Capsulit is a company leader manufacturer of caps and safety closures for the pharma industry. Established in the pharma market since more than 60 years, Capsulit can rely today on a stable collaboration with more than 500 customers, from the main multinational companies, to medium sizes enterprises and to small laboratories. Main skills of Capsulit are: quality service and flexibility. Main products are: pilfer proof caps in aluminium and plastic Child Proof version, caps for injectables solutions, medical devices as measuring cups dosing spoons, droppers and caps for monodose drinkable solutions
BioServices is a global provider of high-quality services in the field of
custom microbial process development and manufacturing. We offer dedicated
solutions for proteins, (high-value) small molecules and microorganisms for
applications in pharma, food, feed and bio-industrial markets.
We are the largest, independent, beta-lactam free microbial contract manufacturing facility in Europe. Our facility is located near Naples, in the south of Italy and has a total fermentation capacity of about 1400 m3 which is spread over two separate fermentation areas. Our associated downstream processing capabilities are spread between multiple, isolated recovery and purification plants with a large diversity of unit operations capable of handling multiple projects in parallel. Recently, we have significantly expanded our spray-drying capabilities, up to pharma API grade.
For more than 50 years, we have built a track record based on our extensive experience in working with a variety of bacterial, yeast and fungal systems. We offer our development and manufacturing services from lab (2-15 L), to pilot (3 m3) to industrial scale (3 m3 - 100 m3).
We have dedicated areas for pharmaceutical manufacturing as well as food-grade manufacturing and comply to cGMP (FDA and EMA approved), GFSI (FSSC 22.000) and ISO standards (14001). Our teams operate on a 24-hour, 7-days/week schedule throughout the year.
Carbosynth are the global supplier of carbohydrates, nucleosides and fine chemicals to the pharmaceutical and bio-tech communities. Our production and laboratories are established in UK, USA and China. Custom synthesis is a growing part of our business in carbohydrates and nucleosides along with our growing capability in fine chemicals.
Carbosynth have diverse and broad experience in chemistries that range from small laboratory scale multi-step synthesis to large scale multi-tonnage manufacture and are able to draw upon a wide range of experience in chemistries and processes, especially in the fields of carbohydrates. This ranges from carbohydrate synthesis to extraction, separation and purification of natural polysaccharides, including monosaccharide building blocks, sugar phosphates, sugars nucleotides, enzyme substrates, oligosaccharides, polysaccharides and glycoconjugates. Carbosynth also offers a range of niche fine chemicals that include versatile building blocks or products with specialist applications ranging from biochemical reagents, natural antioxidants, coupling agents, to activators in peptide and oligonucleotide synthesis.
Carcano Antonio S.p.A is one of the leading company in the aluminium flexible packaging industry.
Situated in the North of Italy, the company covers an international demand of a wide range of industries, from technical to food and beverage, confectionery and, of course, pharmaceutical.
With more than a century of history and a vertically integrated process, Carcano is able to offer various solutions for customers, with the flexibility and know-how to meet the ever-changing needs of the market.
As proof of its innovation boost, Carcano has opened a second new Converting Production Unit in the end of 2016, building on a 15.000 sq m surface area, with state-of-art technology for the production of food and pharma products.
Furthermore, a dedicated pharma slitting and packaging lines are set in a 1.200 sq m Clean Room, certified ISO 8 by TÜV; high quality and safety is guaranteed for all pharma products (blister lidding foil and cold forming, strips and suppositories, etc...).
Carcano fully operates under ISO 14001:2015 and ISO 9001:2015 Bureau Veritas Certifications and in accordance with GMP from aluminium melting to final dispatching, in order to maximize customer satisfaction and the respect for the environment.
The company has more than 450 employees in its 3 Productions Units.
Founded in 2001, Caregen is a global leader of research and marketing of Biomimetic Peptides and Growth Factors. Caregen is not only the company to register Growth Factors in PCPC (Personal Care Products Council, formerly CTFA) but also possesses various Biomimetic Peptide patents all around the world. At Caregen, we value innovations and ideas. With highly skilled in-house scientists and marketing specialists with years of experience in developing and manufacturing of innovative active ingredients, we offer a sophisticated line of purified Biomimetic Peptides and Growth Factors at affordable prices, which is made possible from our mass production technology, enabling our current and prospective customers to have the advantages that they always needed. Additionally, we offer customized Biomimetic Peptides and toll manufacturing services that will provide our customers the solution to their research and manufacturing challenges.
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.
Catalysis, S.L. born as a private and independent company that strives for research and development of products in the cosmetic and dietetic fields. Our scientists are working on finding new food supplements and dermo-cosmetic products that help to improve people´s quality of life.
Cayman Pharma is the world's most reliable source of prostaglandin Active Pharmaceutical Ingredients (APIs) using its own patented route to manufacture APIs for erectile dysfunction, ophthalmic, veterinary, and vascular applications. Cayman Pharma has an excellent track record with over 30 years of experience and an outstanding record of regulatory compliance.
Cayman Pharma was formed in October of 2006 by the merger of two companies with very different geographic origins. Both, however, had unparalleled experience and expertise in Prostaglandin Chemistry. One was Cayman Chemical, a research biochemical company with global recognition as an expert in the field of lipid chemistry. The other was NeraPharm, a company located within the Spolana complex north of Prague since the late 1970s, but only operating as an independent legal entity since 2002. NeraPharm was conceived during the era of Soviet economic domination and central planning. Their goal, which was largely achieved, was to implement independent production of important veterinary prostaglandins for the entire Eastern Bloc. Cayman had its beginnings just a few years later, in 1980. Cayman's vision, also largely accomplished, was to demonstrate that naturally occurring prostaglandins from corals could be an economical and versatile raw material. Targeting the research community instead of the human and veterinary market, Cayman was soon selling a wide variety of extremely pure and valuable prostaglandin standards.
Cayman Pharma represents the joining of almost 60 years of experience with prostaglandin synthesis and biochemistry. NeraPharm brings to the new company a deep understanding of GMP manufacturing under US FDA and EMEA standards, and many years of experience supplying pharmaceutical grade active ingredients. The Czech company also provides Cayman with a tremendous boost in manufacturing capacity. Cayman, on the other hand, brings cutting edge knowledge both in the research field and in GMP methods for the most advanced prostaglandin compounds. Drug candidates for newer indications such as glaucoma, male and female sexual dysfunction, and pulmonary hypertension are all part of the Cayman portfolio.
Cayman Pharma will strive to make the best possible use of its joint EU and US GMP manufacturing operations to ensure that the prostaglandin API that the customer needs is properly certified and ready for release.
CB offers its Customers a long time experience of intense activity in the realization of reliable technological solutions in the industry of special automatic, assembly and control platforms.
The high technological content achieved during these years is the outcome of the constant partnership with big worldwide Players. In particular, the results depend on cooperation between CBA technicians, assembly experts, and Customer designers, deeply experts of the product to assemble. This is the winning policy of CB.
The business unit under the brand “CB AUTOMATION” specializes in automatic assembly platforms with specific focus on medical, pharmaceutical and cosmetic sectors.
CBDepot is a pioneer in the production of high-quality natural cannabinoid ingredients. The company, with roots dating to 2014, has been a leader in helping to establish legal and quality standards for cannabinoid ingredients and the formulation of cannabidiol derivatives that have a fast-growing presence in sectors including food, cosmetics, pharmaceuticals and other health products.
- Three decades focuses on tools, molding, automatic assembly and equipment.
- Extensive and in-depth knowledge and skills on wide-range of medical devices.
- Intensive strengths on pen injectors and drug delivery systems.
- Flexible OEM, ODM manufacturing and production capability.
- Up to date QA, RA and patent intellectual systems.
Founded in May 1989, CCCMHPIE is the leading and most influential national trade associations in China with a mission to promote the international trade and cooperation in medicinal and health products. CCCMHPIE, directly under the Ministry of Commerce of China, has a diverse membership of more than 2400 companies. The fields that CCCMHPIE cover range from Traditional Chinese Medicines (TCM), pharmaceuticals, preparations, medical devices and equipment, dressings, biopharmaceuticals, nutraceuticals, functional cosmetics to health products.
CCPIT Sub-council of Chemical Industry and CCOIC Chemical Industry Chamber of Commerce are the branch organizations of CCPIT and CCOIC. They belong to China Petroleum and Chemical Industry Federation (CPCIF) and work as the CPCIF Conference and Exhibition Department. CCPIT Sub-council of Chemical Industry is a certified member of UFI and Shanghai Convention & Exhibition Industries Association (SCEIA).
We aim to promote trade, economic and technological cooperation between foreign countries and China. Based on serving the entire chemical industry and our member companies, we will make the best efforts to promote the development of chemical industry.
Organizing exhibitions and conferences is our main channel of promoting domestic and overseas economic and trade exchange, however, we organize domestic enterprises to go abroad, hosting and participating in professional chemical industry exhibitions.
CEFALY Technology is a Belgium-based company, specializing in electronics for medical applications. It has developed a preventive and acute migraine treatment so-called Cefaly®. Cefaly® is an external cranial neurostimulation device, It is applied to the forehead using a self-adhesive electrode positioned bilaterally over the upper branches of the trigeminal nerve which is involved in migraine mechanism. The Cefaly® generates very precise electrical impulses allowing to stimulate the trigeminal nerve. Evidence-based for a preventive therapeutic effect as well as for an abortive effect. The efficacy/safety profile is excellent exceeding that of most anti-migraine medication. It fulfills the unmet needs of the migraine medication and therefore it can be offered to patients in whom anti-migraine drugs are not tolerated or contraindicated, and it can be combined with those medications.
Celon Labs is a fully integrated bio-pharmaceutical company with core competencies in the Oncology, Critical Care, Gynecology, Urology & Nephrology segments. At Celon, we aspire to be a specialty pharmaceutical company where quality is a deliverable, formulations are innovative, products are affordable, with a reach transcending all boundaries.
Cenexi is a contract development and manufacturing organization (CDMO) with a strong reputation for fill-finish expertise, innovation and high quality products. Founded in 2004, Cenexi has four production sites in France and Belgium, offering formulation and all services supporting cGMP production of oral solid dosage forms, syrups and suppositories, and liquid or lyophilized steriles. Expansion to a fourth site in 2017 grew Cenexi's specialization in liquid and lyophilized products in vials and pre-filled syringes, including oncology drugs. The longstanding know-how at our sites supports an excellent compliance record and registration to supply product to 115 countries.
Centaur is the largest manufacturer and exporter of Psychotropic APIs to more than 95 countries, including regulated markets. Centaur is approved by USFDA, EUGMP, COFEPRIS, ANVISA, KFDA, TGA, WHO-GMP. The facility also holds 'Accreditation Certificate of foreign drug manufacturer' issued by PMDA, Japan. Centaur holds 15-CEPs and 17-USDMFs. Centaur's R&D is also approved by Department of Science and Technology, Government of India. Centaur's LifeSan is a professional CRO providing services of BA/BE and Clinical Trials. Lifesan is USFDA/UKMHRA inspected and accredited by DCGI, BfArM, MCC and BPFK. Products include: Psychotropics, Ophthalmics, General APIs, Intermediates, CRO and CRAMS Business.
Central Glass Group is specialized in all about fluorine chemistry. We can do various reactions with a great quality management and waste treatment system. We supply fluorine chemicals with gram scale to ton-scale, cGMP if necessary. We are very confident in our innovative reactions and we do hope that our competence is surely of your help. Our global coverage (Japan/US/Europe) can satisfy you with quick response and good customer care. If you need fluoro compounds, please contact us!!
Centurion Pharma is a Turkish Company located in Istanbul and began its journey in 1949. The core business is importing, developing and manufacturing products directed towards use in treatment of chronical and rarely encountered diseases. The product portfolio range consists of:- Biological plasma products -Biosimilar products -Hospital products -Vaccines. Centurion Pharma, which believes that every patient deserves modern treatment alternatives and high quality of life, invested in special R&D projects in the last 5 years, and it has taken a giant step for specific and special products to be manufactured in Turkey. Centurion Pharma embraces respect for both Humans and Nature.
Century Pharmaceuticals Ltd is in the business of manufacturing APIs for over three decades. We offer various kinds of services in addition to supplies of APIs, we undertake long-term contracts for manufacturing intermediates and development of new Active Pharmaceutical Ingredients as per your requirement. We have a sharp focus on giving value added services to our customers cost effectively.
We are supplying APIs to the global pharmaceutical companies in India and abroad since the last 3 decades. Some of our major customers operate in India and export to their products to other countries. Our customers like Teva Pharmaceuticals, Jubilant, Glenmark, Hetero Drugs, Macleod, Abbott, FDC, Wallace Pharma, Intas Pharmaceuticals, Cipla, Aristo pharmaceuticals and other Indian players in the Pharmaceutical industry source their APIs from us regularly.
As a Pharmaceutical company, we manufacture all the APIs which were developed in our own R&D. Currently our R&D is involved in the development of few more API products. We have a Biotech drug discovery R&D jointly developed with an Israeli partner for the development of Recombinant fusion proteins for the treatment and cure of asthma and Mastocytosis.
Cerbios-Pharma SA is a privately held company located in Lugano, Switzerland, specialized in the development and manufacturing of chemical and biological APIs.
A reliable, skilled and highly experienced Hungarian API producer. In its cGMP conformant production plant in Budapest, Hungary, CF Pharma produces high quality active pharmaceutical ingredients and supplies the products to leading generics producers worldwide.CF Pharma was founded by Dr. Géza Schneider in December 1996. Within the next three years a modern production site was established. The first intermediates were manufactured in July 1999.After the first successful inspection by the National Institute of Pharmacy in 2003, a series of Active Pharmaceutical Ingredients with GMP certificates have been developed and produced, establishing CF Pharma as a reliable, skilled and highly experienced Hungarian API producer.The first certified APIs were Lamotrigine, Atracurium and Bicalutamide. In 2009, the site was also successfully inspected by the FDA. Today CF Pharma employs 100 people and is serving many leading generics producers in all part of the world.
CFM Co Farmaceutica Milanese SpA (founded in 1949) supplies raw materials and active ingredients to the pharmaceutical, nutritional and cosmetics industries in Italy and worldwide. The company proposes safe products to its customers and scouts for new sources and opportunities for them, in various parts of the world. CFM is ISO 9001:2008 certified and operates according to GDP (good distribution practice). The company also offers a qualified distribution point to companies wishing to distribute their products to Italy.
CG Pharma & Nutrition is a globally active GMP-manufacturer and GDP-distributor of pharmaceutical starting materials, Excipients and API. We are holder of a Drug Manufacturing Authorization according to German Medicinal Products Act.
Our product portfolio covers more than 650 raw materials for the pharmaceutical industry.
We are able to formulate and produce solid and liquid dosage forms under clean-room conditions (C&D). Mixing tanks, milling plants, sieve systems and silos are available for additional processing and re-packing steps. We manufacture aqueous solutions of starting materials, Purified Water (AP) and Water for Injection (WFI) according to EP/USP.
The Chanelle Group is a group of companies involved in the development, manufacture and distribution of human and veterinary pharmaceuticals and related services. The group is headquartered in Co. Galway, Ireland, where its principal operations are based. Chanelle Medical has offices in Paris, UK and Jordan. The group was founded in 1983 by Michael H. Burke and has expanded and developed significantly since then.
ComWin is specializing in producing and distributing APIs, intermediates & animal healthcare products. Our main products are 5-Chloro-2-pentanone, 2-MeTHF, Cyclopropyl Methylketone, Orlistat, Rosuvastatin Calcium, Fipronil, Cloprostenol Sodium. International logistics services is our highlighted strengths, like cold-chain, hazardous shipment, door to door, which we've been providing to Merial, Vetoquinol, DKSH, IMCD. .
Changzhou Haijiang Drying Equipment Company produce more 1000 sets of all kinds of drying, mixing, granulating, crushing, sieving and so on equipment annually. And this company has become a important and key enterprise in drying industry of China within several years and is at the leading place in the same industry.
Changzhou Yabang-QH Pharmachem Co Ltd specialises in R&D, manufacturing, sales and marketing of Anthelmintic products.
We also jointly founded Jiangsu Provincial Engineering & Technology Research Center for Animal Use Anthelmintic Drugs, with the local government, specializing in the R&D of Anthelmintic Products.
Chematek SpA is a chemical company dealing with fine chemicals, intermediates and additives for a diversified range of industries such as pharmaceuticals, cosmetic, food, metal finishing/electroplating, textile, agrochemical, petrochemical, specialty chemical. Chematek sells worldwide through a capillary network of salesman and agents and has offices in Italy, France, UK, China and India. Chematek S. P. A. (www. Chematek. Com), worldwide exclusive distributor for SynhydridTM (bis(2-Methoxyethoxy) sodium aluminum hydride 70% solution in toluene) announces the expansion of production facilities for Synhydrid. This is part of Chemateks overall plan to enhance its long-term tradition in reducing agents like sodium borohydride, sodium cyano borohydride, etc.
ChemCon is a Contract development and manufacturing organization (CDMO) producing specialty chemicals, advanced excipients, and drug substances on demand to your specifications. Our products are used worldwide for pre-clinical development, during clinical trials and as commercial drug substances. We specialize in transferring research and development projects from chemical synthesis development, via process scale-up and validation, into fully cGMP-compliant processes. Everything is handled under one roof from preclinical to commercial material. Our facilities are optimized for the production of gram to multi-kilogram quantities. We also offer external analytical services, independent from production services.
Chemcon is a leading manufacturer of Pharmaceutical intermediates and Oilfield Chemicals (Completion Fluids). At Chemcon, an ISO 9001:2015 certified company, we manufacture all our products complying GMP guidelines and completion fluids of unmatched purity, complying with highest standards (API-RP-13J) of quality in Oilfield Industry.
Chemi SPA has
relevant expertise in the area of Low Molecular Weight Heparins,
Polysaccharide Derivatives, Peptides and Oncology Products.
Pipeline of several technology-innovative products and generic Finished Dosage Forms with granted Marketing Authorizations and dossiers available for licensing
CHEMINEAU has been the specialist for 40 years in the contract manufacturing of sprays, liquids and creams. Successful and longlasting partnerships with French and Foreign companies are the best proof of CHEMINEAU's expertise. Located in Vouvray in the Loire Valley in France, CHEMINEAU ISO 9001 certified pharmaceutical facility of 15000 m2 provides customers skilled staff, a strong structure and services to guarantee security, quality, attractive prices and competitive lead times. From analytical and galenic development with ICH norms (pilot, clinical batches, stability tests, validations, CTD files) to industrial transfers (regulatory, technical and logistics aspects), from components purchasing to pharmaceutical release, CHEMINEAU offers a complete range of outsourcing solutions.
Since the 1950's, we have been dedicated to providing the pharmaceutical market with high quality phosphate based excipients for the manufacturing of liquid and solid dosage forms. Continuous development and improvement of our products, exclusively manufactured in Germany following current Good Manufacturing and current Good Distribution Practices, make us a unique partner and ensure the best solutions for your business. Beside proven quality by our customers and by independent third-party certifications, we have earned our reputation by a close collaboration with our partners, which includes technical service and regulatory support. This long-term commitment is an additional incentive for us to continueto focus on customer oriented solutions.
We are a manufacturer of API's and Formulations in India and we export to Japan, China, Indonesia, North America Latin America and African sub-continent. Our facilities are WHO/EU GMP approved and we are an ISO 9001-2008 compliant company.
We have established finished formulation lines in South Asian and Latin American countries. It is our vision to achieve worldwide recognition as an excellent business partner from India by providing our customers with superior quality products at highly affordable prices and following that up with reliable service consistently, thereby giving them an unparalleled experience.
One of our finished formulation unit caters to Pfizer, Glaxo Smith Kline, Nicholas Piramal, Ranbaxy, Dr. Reddy's, Abott, Merck, Novartis, US Vitamins, Wockhardt, etc. for the domestic market in India.
We also have a USFDA approved unit manufacturing food colors for human consumption.
Pharmaceutical finished formulations from WHO/EU GMP units are registered/being registered in 26 countries including Peru, Panama, Ecuador, Chile, Curaçao, Suriname, Haiti, Aruba, Trinidad and Tobago, Philippines, Myanmar, Laos, Malaysia, Thailand, Indonesia, Hong Kong, Vietnam, Sri Lanka, Maldives, Brunei, Nepal, China, Russia, Croatia, Venezuela and Bhutan.
Mission & Vision
Chemsphere Technology Inc. is a professional chemistry player in Taiwan. We specialize in specialty and fine chemical. Our customers spread to the electronic industry, the pharmaceutical industry, the biotech industry, and the chemical industry.
We have partnership with many R&D centers in Asia and Europe, such as Korea, China, India and Germany. We certainly offer a large library of compounds and also provide the custom chemical synthesis. We are keeping exploring our business all around the world.
Chemsphere is a specialty pharmaceutical/nutraceutical raw materials company with strong formulation development techniques and high-quality Active Pharmaceutical Ingredients.
We are committed to offer:
1. Multiple products in MRI contrast media, from APIs to finished products.
2. Tetrahydrobiopterin Dihydrochloride from intermediates, APIs to finished products.
3. cGMP Cholesterol(vegetal-derived, semi-synthetic)
4. Astaxanthin(high purity)
5. Serum-Free Medium for Virus production
6. L-Glutathione(Reduced GSH)
7. CMO/CRO service
Chemtrade is the only North American manufacturer of API grade KCl. Our potassium chloride product is supplied globally and is available in Custom morphologies (spheres and cubes) for sustained release or immediate release application. Chemtrade's KCl is currently compliant with USP/EP/FCC/JP/BP and ACS monographs. Chemtrade also manufactures high purity compendial grade (NF/BP/JP/EP/FCC and ACS) KOH and NaOH pellets which are used as excipients for pH adjustment and buffers. Additionally Chemtrade is one of the largest North American manufacturer of aluminum based adjuvants for vaccines and plasma protein separation.
Chemwerth is a full service generic drug development and supply company with offices in the U.S., China & India that delivers high quality APIs to regulated markets worldwide. Chemwerth provides expertise in research & development; technical and regulatory services; sales & marketing; and strong project management providing customers with speed to market advantage.
With a 45 year track record of serving the healthcare sector, Zhejiang Cheng Yi Pharmaceutical Co Ltd has established itself as a reliable manufacturer and supplier of pharmaceutical products and a contract manufacturing partner to the pharmaceutical industry. At Cheng Yi pharmaceutical, we dedicate our operational efforts to manufacturing excellence, strict compliance with cGMP requirements, and customer satisfaction. Our API manufacturing facilities were first audited by TGA in 1998, and have since been regularly inspected and consistently approved by other world regulatory authorities. In particular, we are proud of the success in the first-ever global joint audit of our facilities by FDA, EMEA and TGA in 2010. Our business comprises development, manufacturing and supply of APIs, pharmaceutical intermediates and dosage form products. Headquartered on Dongtou Island of Zhejiang Province and with sales center in Shanghai, Cheng Yi Pharmaceutical employs 560 and operates 2 manufacturing sites with total site area of 225000 sq meters, total reactor capacity of 451 cubic meters and fermentation capacity of 300 MT, as well as 2 dosage form production lines.
Chengda Pharmaceuticals Co Ltd was set up in 1999, located in the beautiful scenery of the Hangzhou-Jiaxing-Huzhou plain, Jiashan Economic Development Zone. Nowadays the company owns two plant sites, located in No.5, Hengshan Road and No.36, Huanghe Road
The company mainly produces APIs, food additives, feed additives, antibiotics, anticancer, antiviral of pharmaceutical intermediates, and etc. Products are sold in more than 30 countries and regions. The in-house developed product, Levocarnitine, has won the honorary title of “national, key and new product” and passed the US FDA on-site inspection without deficiency in March, 2013.
Chengdu Easton Biopharmaceuticals Co Ltd is a new leading pharmaceutical company, engaging in development, manufacture and distribution of commercial-scale Finished Dosage Forms (FDFs) and Active Pharmaceutical Ingredients (APIs). Our manufacturing facilities are fully compliant with EU-GMP and US-GMP standards.
Our products include Bisoprolol Fumarate, Clopidogrel Bisulfate, Flupirtine Maleate, Naloxone Hydrochloride, Olanzapine, Prasugrel Hydrochloride, Moxifloxacin Hydrochloride, Vilazodone Hydrochloride, Esomeprazole(sodium/magnesium), Fusidate Sodium etc.
We are Fmoc-amino acids and chemical reagents manufacturer.We keep each Fmoc 200kg in stock,yearly output of Chemical reagents is over 30000T.
Chengdu Pukang Biotechnology Co., Ltd. was founded in 2008?it is a high-tech enterprise specializing in unnatural amino acids and derivatives. Pukang can produce PEG series products with high purity and single molecular weight. The main products of the company are PEG series derivatives,Hydroxyproline series derivatives, and peptide long-t1/2 modification drugs.Meanwhile we have important intermediates innovation drugs such as Lifitegrast intermediates and Semaglutide side chain.The quality system is managed according to the GMP standard.
The company is devoted to studying, developing, producing, and marketing the natural herbal medicines and has been bestowed with an import & export license. The products include Hesperidin, Synephrine, Rutin, Berberine Hydrochloride, Chlorogenic Acid, and Raicalin etc.
Chimet produces supported (heterogeneous) and unsupported (homogeneous) catalysts based on PM (precious metals as Pd, Pt, Rh, Ru) , with application in the fine chemical and pharmaceutical industry (APIs). Chimet as recovery & refining of PM leader , offers a complete PM loop service to its customers with the guarantee of a maximum yield and quick settlement on the PM recovery from spent catalyst. Tailor-made catalysts can be produced based on customer's requirements. Many different physical, chemical and catalytic activity tests are available to the customers for the R&D, Quality Control and Technical Assistance.
China Animal Husbandry Industry Co Ltd manufactures and sells animal health products and feed additives in China. It offers various biological products consisting of vaccines for fowls, diagnostic liquid products, avian influenza vaccines, foot-and-mouth disease vaccines, swine vaccines, and others; feedstuffs, such as feedstuff raw materials, feedstuff additives, pre-mixed feedstuffs, and multi-vitamin feedstuffs; and veterinary drugs comprising animal remedy products and drug additives. The company is based in Beijing, China.
With nearly two decades of committed service to the peptide industry, Chinese Peptide Company(CPC) is one of the most trusted providers of high quality peptides for researchers and pharmaceutical companies all over the world. The CPC group is managed by peptide experts who have been actively pursuing peptide design and large scale manufacturing for more than 30 years in the industry. The CPC Group currently employs more than 500 chemists in Hangzhou, China and the United States has achieved many successful US-FDA inspections, ISO-9001 and ISO-13485 certifications. The state-of-the-art peptide facility is uniquely designed to handle research-grade peptides as well as cGMP grade peptides for clinical trials and API development from milligram to hundreds of kilogram scale with its patented high-through-put PeptidEx technology.
- The First US FDA inspected GMP peptide facility in Asia
- CPC is highly experienced at synthesizing challenging peptide sequences and complex modifications designed to your exact specifications
- First choice of many esteemed scientific research institutions and pharmaceutical companies all over the world
- Peptide purity up to 99.9%
- Peptide length up to 200 amino acids
- Quantities from milligrams to hundreds of kilograms
- Wide selection of complex peptide modifications available including long hydrophobic sequences, highly constrained (e.g., macrocyclization, multiple disulfide bridges, hydrocarbon-stapled, etc.) peptides, and custom-designed FRET substrates
- Thousands of known sequences from 100 different peptide categories
- Over 2000 peptide products available from stock
- Catalogue updating regularly with the latest published peptide sequences
- Reference Link: http://www.chinesepeptide.com
- New Chemical Entities (NCE) 1? One-stop development and registration services 2?New Drug Screening; API Development; Regulatory Support, API Commercial Supply
- Generics 1?Generic Drug Development and DMF Filing 2?Commercial Supply
- Capability to handle large scale projects (up to 20kgs per batch )
- Large solid phase and solution phase peptide synthesis reactors (up to 500L)
- 100K, 10K clean rooms
- Regulatory support (China and Overseas)
- Excellent track record with pharmaceutical companies in the world
- CFR 210/211, ICH Q7A
Chiral Quest was founded in 2000, devoted to contract chemical development and manufacturing services to meet demanding at any stage of development (kilo-lab, pilot-plant and full scale commercial).
With headquarters and R&D center located in Suzhou Industrial Park, Chiral Quest has one manufacturing site in Jiangxi province, and three overseas offices in USA, Europe & India respectively. Chiral Quest focuses on R&D, and holds 13 U.S. patents of asymmetric catalysts and ligands; 6 patents of innovative routes for generic drug intermediattes.
Chiral Quest's mission is to create value for global health care industry by using the most economic and environmental friendly methods to produce chiral pharmaceutical intermediates and API's.
Chirogate is a leading US-FDA inspected Prostaglandin (PG) manufacturer and owns more than 6 dedicated & cGMP-compliant production lines for cutting-edged manufacturing of PGs. Several process patents filed and granted worldwide are to provide a commercially revolutionary synthetic approach and an exciting spectrum of advanced intermediates for synthesis of new PG entities. US DMFs filed for Unoprostone Isopropyl, Treprostinil, Latanoprost, Bimatoprost, and Travoprost with additional registration experiences in China, Japan, Canada, Australia, New Zealand and major EU countries. Products: Unoprostone Isopropyl, Treprostinil, Treprostinil Sodium & Dienthanolamine, Latanoprost, Bimatoprost, Travoprost, Misoprostol, Lubiprostone, Epoprostenol Sodium, Dinoprostone, Tafluprost, Alprostadil, Dinoprost (& Tromethamine), and (+)-Cloprostenol (&Sodium).
Chongqing Daxin Pharmaceutical Co., Ltd is the largest manufacturing base of Lovastatin in the world. We own two large-scale pharmaceutical manufacturing bases, including a new base complying with international cGMP standards; as well as owning hundred of APIs, finished dosages and intermediates, including cardio-vascular, antibiotics, immunosuppressant, plasma volume expander, etc.
Chr. Olesen is a worldwide group of partner-driven distribution and manufacturing companies. The company was originally founded in 1885 and is today managed by the fourth generation. Chr. Olesen is active in distributing ingredients and API's in four different business areas: Feed, Food, Pharma and Vet Pharma. Chr. Olesen Synthesis is the Group's manufacturing company. Chr. Olesen Synthesis is based in Denmark and is an expert in developing and manufacturing and registration of high value wet chemical synthesis products like Hydromorphone, Codeine Phosphate, Pramipexole, Terbinafine Risedronate, Tolfenamic Acid, Amphetamine derivatives and advanced intermediates for Buprenorphine and Tamsulosin. Please explore the videos and more information about our esteemed company at our website: www.chr-olesen.dk.