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.
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]
Ajinomoto Bio-Pharma Services is a fully integrated contract development and manufacturing organization, with sites in Wetteren and Balen, Belgium and San Diego, California, USA, providing comprehensive process development services, cGMP manufacturing and drug product fill finish services of small molecule and biologic APIs and intermediates. Ajinomoto Bio-Pharma Services offers a broad range of innovative platforms and capabilities to rapidly scale from clinical and pilot programs to commercial quantities, including: Corynex technologies, oglionucleotide synthesis, antibody drug conjugations (ADC), high potency APIs (HPAPI), continuous flow manufacturing and more. Ajinomoto Bio-Pharma Services is dedicated to providing a high level of quality and service to meet our client's needs. Large Molecule Manufacturing: One of the industry's top leaders in microbial biologic manufacturing, using patented technologies and providing impeccable quality. Highly Potent & ADC Services: Ajinomoto Bio-Pharma Services offers dedicated production and laboratory suites for high containment ADC bioconjugates and highly potent compounds, as well as formulation and fill finish services Oligo & Peptide Synthesis: An industry leader in the synthesis of high quality, scalable, custom oligonucleotides and peptides Drug Product Manufacturing: A leader in aseptic filling, offering a wide range of capabilities for vials and syringes Development Services: Our highly knowledgeable Process Development team will establish and characterize a robust manufacturing process to ensure consistent cGMP manufacturing performance Product Quality & Analytical Services: Our well-designed product quality and analytical programs work to ensure the success of your small and large molecule products through th
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).
AmpleLogic is a leading automation solutions provider for pharmaceutical industry. It has a unique visual development, drag & drop feature with intuitive interface, where 36 data components are available to accommodate data verification & validation which shortens the application development time. Our 21 CFR Part 11 compliant and EU Annex 11 solutions are in use at more than 17 US FDA, 3 MHRA and 10 WHO approved units. AmpleLogic has tweaked traditional V Model to accelerate GMP Automations and address data integrity issues with unique No/ Low Code Platform by adding the Configuration and Experimentation phase in the implementation cycle which address regulatory audit observations related to revalidation, deviations and multiple release managements results in implementation time reduction by 70%. A strong focus in Pharma domain made us to build 14 ready to use apps to fulfill the need of QA, QC and Production area. Our pharma software solutions (QMS Automation, Batch Record Issuance Software, Quality Control Automation, ANDA and DMF Tracker Software, Calibration Schedules Tracking Software, Training Management System, Electronic Batch Recording Software and Artwork Management Software) implemented at US FDA, MHRA and WHO approved manufacturers in most of the Pharma and Life Science sectors. We at AmpleLogic have received 100% user acceptance from our existing customers, which proves NO PROJECT FAILURES till date.
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.
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.
Chemical Company is established in the manufacture of products for
pharmaceutical, healthcare, flavour/fragrance, and other specialised chemical
and industrial applications. Offering chiral chemistry using both chemo- &
bio-catalysis technology coupled with a wide range of modern synthetic
reactions, our competence and experience in process development and
optimisation ensures success in your toll manufacturing and custom synthesis
Avara offers contract manufacturing of APIs, solid and liquid sterile drug product, and packaging from nine world-class facilities. Led by experienced, entrepreneurial industry leaders, 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.
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
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.
Divasa-Farmavic,S.A. is one of the few EU veterinary manufacturers with fully GMP approved facilities to manufacture: >Beta-lactam and non-beta-lactam totally separate production lines for injections/solids: Sterile Solutions, aseptic and terminal sterilization. Sterile Suspensions. Extemporaneous powder for injections. Oral Soluble Powders. Medicated Premixes. >Aerosols >Pets collars >Oral and topic solutions
European Medical Contract Manufacturing B.V. (EMCM) is a centre of excellence in developing and manufacturing sterile medical products for Medical Device and Pharmaceutical companies. At our GMP and ISO accredited and national and international inspected facilities, we focus on the (contract) manufacturing of organic solvents, aqueous solutions, powders, and highly viscous suspensions and gels. We pride ourselves on our flexibility, being able to produce small or large scale batches customised to our customers' needs. The products we currently manufacture can be classified under Pharmaceuticals, Medical Devices and Tissues Grafts. Be it ampoules, vials, syringes, pouches, bottles or blisters, we support opportunities that enable our customers to bring their innovations to the market.
Fareva is a global pharmaceutical and API leading CDMO, with 10.000 employees in 35 sites (Europe, Russia, Turkey, Americas). Fareva offers flexible solutions for analytical and dosage forms development, clinical trials, regulatory services, and manufacturing of liquids, suspensions, semi-solids, solids, high potents, injectables, ophthalmics, aerosols medical devices, food supplements...
With revenues of € 130 Millions expected in 2018, approximately 1200 SKUs and more than 500 employees, Fine Foods & Pharmaceuticals NTM's is a Contract Development and Manufacturing Organization with no proprietary brand, producing Pharmaceuticals, Dietary Supplements and Medical Devices in solid oral forms. The three manufacturing sites are located in Zingonia, (Dietary Supplements and Medical Devices), Brembate and Nembro, (Pharmaceuticals), all a few miles from Bergamo, Northern Italy. 92 manufacturing lines produce powders, granules, capsules and tablets, packaged in jars, sachets, sticks, blisters, strips and bottles. The main factor of the success of Fine Foods has been an unrelenting quest for quality and customer's satisfaction, combined with an obsessive attention to ethics and to its own human capital. Fine Foods has invested heavily on quality, intended not just as the product's quality, but as a model of overall sustainability and is complying with the highest industry standards: ISO 9001:2008, ISO 22000:2005, ISO 13485:2012, ISO 14001:2004, OHSAS 18001:2007, GMP for Food Supplements, SMETA, D.Lgs 231. A significant customer's loyalty and a markedly low turnover of personnel are undoubtable evidence of a company with a solid reliability and extremely attentive to internal and external customers. Additional information is available at http://www.finefoods.it/en/
Fresenius Kabi Product Partnering, the contract manufacturing platform of Fresenius Kabi, offers manufacturing expertise of over 30 facilities worldwide. We offer the full range of services for fill/finish of solutions and emulsions in ampoules, vials, bottles, IV-bags, and pre-filled syringes. Our manufacturing facilities are registered by all regulatory bodies worldwide.
Genovior Biotech Corp. is a vertically integrated contract development and manufacture company, providing following services:
(a) process development of peptide or protein biologics from microbial or human recombinant fermentation processes
(b) formulation development of biological injectables
(c) manufacturing capacities of biologics, lyophilized injectable, and prefilled syringe/cartridge for preclinical, clinical, and commercial uses
Genovior is a dedicated CDMO focusing on providing high quality products at a competitive cost under cGMP and PIC/S for our customers worldwide. Our facilities fully comply with the regulations of FDA, EMA and other agencies, our one-stop services conveniently provide effective and efficient solution and our non-competition policy provides maximum security and protection in IP for our clients.
Getz Pharma is world-class branded generic pharmaceutical company with a global outlook. The company's mission is to develop, produce and market safe, effective and quality medicines and healthcare products that will improve the health and quality of life of men, women and children. Getz Pharma manufactures and markets brands trusted by healthcare professionals around the world. The products are manufactured at Getz Pharma's state-of-the-art manufacturing facility that is pre-qualified by World Health Organization (WHO), Geneva and a member country of Pharmaceutical Inspection Co-operation Scheme (PIC/S). The company currently operates in more than 25 countries in South Asia, Central Asia, South East Asia and Africa. It provides high quality and affordable healthcare solutions in the areas of Cardiometabolics, Hepatology, Gastroenterology, Pulmonology, Urology, Gynecology, Orthopedics & Rheumatology and Infectious Diseases. IMS rates Getz Pharma as one of the fastest growing pharmaceutical companies within most countries where it operates.
Headquartered in Hyderabad, India, GVK Biosciences is one of Asia's leading Discovery Research and Development organizations. GVK BIO provides a broad spectrum of services, across the Research and Development and manufacturing value chain with a focus on speed and quality. GVK BIO capabilities include Integrated Programs, Discovery Services, Clinical Development, Contract Manufacturing, Formulations and Informatics. GVK BIO's 2400 employees serve a diverse and global customer base of more than 350 satisfied customers.
HERMES PHARMA is the expert in developing and manufacturing user-friendly oral dosage forms. We offer customized solutions at every point along the pharmaceutical value chain, from the development of new product concepts and formulations to manufacturing and regulatory support. For more than 40 years, leading healthcare companies around the globe have been working with HERMES PHARMA to expand their product lines and grow their brands. HERMES PHARMA is a division of Hermes Arzneimittel, a leading German provider of high-quality medicines, food and dietary supplements marketed under its proprietary, well-established brands.
With its core competences in its business areas
laboratory services, reference standards as well as vigilance and quality
services, HWI pharma services GmbH offers
are wide range of services for the pharmaceutical industry. We have more than
25 years of experience in analytical method development and validation, trace
analysis, troubleshooting, quality control and stability testing of APIs,
excipients, and medicinal products as well as substance-based medical devices
and medical devices. We have a certificate of GMP compliance and a
manufacturing authorisation for the release testing of clinical and commercial
batches. Our reference standard concept ranges from a wide selection of
qualified primary reference standards and working standards to the complete
just-in-time supply to quality control laboratories. We have our own
GVP-compliant pharmacovigilance system and offer comprehensive support concerning
the safety of medicinal products and medical devices.
Along with the product development of HWI development GmbH and the regulatory services of i.DRAS GmbH, HWI group offers a wide range of services for APIs, medicinal products and medical devices from one source.
IntelGenx is a Leader in Pharmaceutical Film Development & Manufacturing. Our mission is to Make Approved Drugs Better, with next generation pharmaceutical products that address unmet medical needs, and offer significant benefits to patients and physicians. Our film proprietary technologies, VersaFilm™ and VetaFilm™, enable the development of pharmaceutical oral films with potential to improve absorption, accelerate onset of action, reduce side effects, ease administration and improve patient compliance. IntelGenx' highly skilled team provides comprehensive pharmaceuticals services to pharmaceutical partners, including R&D, analytical method development, clinical monitoring, intellectual property, regulatory and manufacturing services. We Offer: • Development and Manufacturing by Contract and • Licensing-Out of Innovative Oral Film Products. Our teams of experts are committed to go above and beyond to satisfy the needs of our partners.
LABIANA GROUP is a contract manufacturing organisation with two manufacturing plants located in Barcelona producing medicines for human and animal health. We manufacture a complete set of solid forms and sterile or non-sterile liquid products including freeze dried. We can also offer integrated services like formulation and dossier development, pilot batch production, packing, chemical and micro-biological quality control or validations.
We are focussed aswell in :
PROBIOTICS FOR HEALTHCARE PRODUCTS , FOOD SUPLEMENTS , COSMETIC, SEVERAL HUNDRED FORMULAS WITH MORE THAN 3.000 STRAINS IN OUR PRIVATION COLLECTION.. VAGINAL INFECTIONS,INTESTINAL HEALTH OF ADULTS,DEPRESSIVE SYMPTONS, BABY, REDUCTION OF ANTIBIOITIC-ASSOCIATED SIDE-EFFECTS.. DIABETES CARE.- DIVISION UNDER CONSTRUCTION- ANTIDIABETDRUGS- MEDICAL DEVICES, INSULIN PEN NEEDLES, STRIPS GLUCOSE -METTERS….. ANAESTHETIC CARE- VECURONY BROMIDE
Dynamic, independent, family owned group. Six manufacturing sites in France, 15 BFS machines for production of sterile unidose vials, worldwide distribution network. CMO for pharmaceutical products, medical devices and cosmetics
Lichtenheldt is the committed full service pharmaceutical contract manufacturer and developer for non-sterile liquid and semi-solid dosage forms. Our manufacturing plant is accredited according to EU GMP and DIN EN ISO 13485 for medical products. Lichtenheldt has an ex proof production zone, store capabilities. Production and packaging under protective atmosphere is also possible. Our packaging expertise ranges from bottles, tubes, canisters to IBC bulk containers. In addition to our manufacturing service we offer a wide range of additional service like analytical testing, galenic development, feasibility studies and regulatory services. Lichtenheldt has over 30 years of experience as a trustworthy contract manufacturer. We are the CMO-Expert for liquid and semi solids production and a first choice strategic outsourcing partner, so let's come together.
For over 30 years, Lonza has been helping emerging and
established pharmaceutical and biotech companies increase product quality,
improve production processes, navigate development and regulatory processes,
lower the cost of goods and get to market faster. We help our customers advance
therapeutics through the clinical pipeline and to the patient.
With over seventy years of experience, OFI is one of Europe's foremost companies in the development and manufacturing of dermo-cosmetic, dietary-nutritional products and medical devices; the company is considered the Italian leader in the production of liquid forms Quality, reliability and a powerful innovative drive are the strong points recognized by the market and professionals in the sector. OFI operates with the highest standards, like ISO certifications (9001, 14001, 22716), Ohsas 18001, Halal, FDA approved, ICEA – Eco bio cosmetics, GMP. OFI has a strong know-how in Research and Development, working and proposing new formulation and innovativion to big cosmetic and pharmacuetical companies. OFI brands therefore offer products that are very advanced, innovative and anticipate trends. Clinical tests also prove the effectiveness of several products. OFI proposes several product types and packaging solutions, Full Service from idea generation till distribution, highest standards, like ISO certifications, Ohsas 18001, FDA, GMP, ICEA OFI produces and commercializes also its own brands: Bottega di LungaVita, Euronatural and Kosmida Bottega di LungaVita - www.bottegadilungavita.com- creates natural products by cleverly combining age-old traditions with scientific innovation. Where nature meets science, is supported by research and shapes the elegance: there stands Bottega di LungaVita. Ancient traditions and new technologies, on-going commitment to respect the environment and create natural but effective products, make Bottega di LungaVita very appealing to the natural and organic trends increasing in all markets The brand is sold in Italy in herbal and natural shops, pharmacies and para-pharmacies. It is also distributed abroad in several countries Euronatural - www.euronatural.it - offers a wide range of dietary supplements for our daily well-being. Vitamins, probiotics, Iron and folic Acid, Omega 3 among others, mainly in liquid forms and in practical mono-dose liquid sachet, easy to carry and easy to use. Kosmida - www.kosmida.com - is dedicated to the treatment of dermatological problems; it uses natural active ingredients in accordance with the most recent discoveries in the field of bio-medical and dermatological research. Kosmida provides cosmeceutical products, formulations not only rich in functional active ingredients but also dermal affinity.
Particle Sciences, a Lubrizol LifeSciences company, is a leading Contract Development and Manufacturing Organization (CDMO) specializing in complex drug products. Most drug products being developed today face one or more technical challenges. Whether dealing with a new chemical entity or reformulating an existing active pharmaceutical ingredient (API), the product's therapeutic and commercial success depends on the choice of the right drug delivery system and development partner. We provide seamless support for our client's drug product by combining our extensive formulation and physical characterization capabilities with state-of-the-art analytical, bioanalytical, and clinical and commercial manufacturing services.
Thermo Fisher Scientific Pharma Services provides end-to-end development and manufacturing solutions to customers of all sizes through Patheon and Fisher Clinical Services. With more than 40 locations around the world, the company has extensive capabilities including, drug substance and product development, clinical trials and commercial-scale manufacturing. Thermo Fisher Scientific Inc. is the world leader in serving science, with revenues of more than $20 billion and approximately 70,000 employees globally. Our mission is to enable our customers to make the world healthier,cleaner and safer. We help our customers accelerate life sciences research, solve complex analytical challenges,improve patient diagnostics, deliver medicines to market and increase laboratory productivity. Through our premier brands – Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific and Unity Lab Services – we offer an unmatched combination of innovative technologies, purchasing convenience and comprehensive services.
PCI is an integrated full service provider and a trusted partner to leading companies in the global healthcare industry; we offer unparalleled expertise and experience in taking compounds from the earliest stages of development through to commercial launch, delivering speed to market and commercial success for our customers.
Core services include: Analytical services, formulation development, clinical trial supply, commercial manufacturing and packaging, QP services, supply chain management, storage and distribution. Customers can choose to use us as a complete development partner and benefit from our full range of services or choose any of our core services as a stand-alone offering.
The core expertise of Pierre Fabre CDMO is the fill & finish of injectables products, now completed with the manufacturing of clinical batches of biotech molecules (mAbs, ADC). PF-CDMO also proposes the development and commercial production of APIs and nutraceutical ingredients, and oral products, such as liquids, tablets and pharmaceutical lozenges.
We are dedicated to accelerating the development of new drugs for patients around the world. We provide formulation development, clinical pharmacology trials, and clinical and commercial manufacturing services to the pharmaceutical and biotech industry. These services are provided either individually or as an integrated service offering via our Translational PharmaceuticsÂ® platform.
R-Pharm Germany GmbH is a reliable CDMO, covering a wide range of manufacturing and packaging solutions for solid dosages. The state-of the-art location based in Southern Germany is approved by all major authorities (US FDA, EMA, ANVISA, Korean FDA, NAFDAC, Turkish MOH, Saudi-Arabia, etc.) and offers cost-effective services on all supply-chain steps (development, scale up, production, analytics and stability). Highlights: Serialization and Aggregation Readiness & 15 years of experience in high potent manufacturing Our full-service-competences will transform your ideas to a product - ready for the world market.
Recipharm is a leading contract development and manufacturing organisation (CDMO) headquartered in Stockholm, Sweden. We operate development and manufacturing facilities in France, Germany, India, Israel, Italy, Portugal, Spain, Sweden, the UK and the US and are continuing to grow and expand our offering for our customers. Employing around 5,000 people, we are focused on supporting pharmaceutical companies with our full service offering, taking products from early development through to commercial production. For over 20 years we have been there for our clients throughout the entire product lifecycle, providing pharmaceutical expertise and managing complexity, time and time again. Despite our growing global footprint, we conduct our business as we always have and continue to deliver value for money with each customer's needs firmly at the heart of all that we do. That's the Recipharm way. For more information visit www.recipharm.com
RIEMSER Pharma GmbH is a
speciality pharmaceutical company established in December 1992 with core
competencies focused on targeting therapy areas with high unmet medical needs.
RIEMSER markets its own product portfolio in numerous therapeutical areas including oncology, neurology, antiinfectives and dermatology. RIEMSER's success is attributed to the effective acquisition and licensing of products adding significant value to its distribution channels which spans over 60 countries with more than 300 approvals worldwide. As a result of the extensive experience and vast market knowledge, Riemser has successfully submitted and received 30 approvals over the past two years.
With strategic acquisitions in Europe, RIEMSER has progressively enhanced its expertise and competencies in the core markets.
Our company has a long time experience in developping and producing innovative solutions for patients. With a business unit dedicated to Contract Manufacturing services and a global manufacturing network, we can bring this expertise to partners looking for a different kind of relationship. We focus on quality, reliability and efficiency. We have a competitive edge due to being a 60+ years old independant group, which is now governed by a foundation. Servier #CDMO offers a comprehensive integrated range of services embedded to protect your molecule through clinical and commercial manufacture, from lab to pilot batch through scale-up to marketed product manufacturing, including industrial preparative chromatography to speed up your time to market. The benefits in choosing embedded services from Servier CDMO: • Leading pharmaceutical know-how • Proven quality track record • Experience and understanding of project objectives • A streamlined regulatory pathway • Global flexibility with 16 manufacturing sites • More than 50 products commercialized over 60 years • 27 billion units of drug product manufactured annually • 21,600 employees, with 3,000 in Industry • Present in 148 countries
Our Life Science Services provide analytical, bioanalytical and clinical trial testing capabilities, along with process management, that enable pharmaceuticals to swiftly reach those that need them with minimal cost and maximum safety. We partner with the pharmaceutical, biopharmaceutical, biotechnology, medical device and healthcare-related industries to provide a wide range of essential services.
Skyepharma is the oral solutions business unit of the Vectura Group of companies [leader in Drug Delivery Inhalation] and is a key player in drug development and delivery of oral technologies serving the global pharmaceutical, biotech and consumer health industries. As an integrated CDMO, Skyepharma's controlled-release technologies and oral solids capability offer development, manufacturing and packaging of classic and complex oral solid dosage forms: - Single layer tablets - Multi-layer tablets - Tab-in-tab - Tab-in-caps - Hard gel capsules - Sachets . [Visit our webiste : www.skyepharma.fr and Follow us on LinkedIn.]
Solchim S.r.l., part of the Volcke Aerosol Connection, offers complete aerosol and spray system solutions for cosmetics, healthcare products and medical devices. We work together with partners and customers world-wide to successfully bring our products and tailor-made formulations to the customer. We conform to ISO 9001-2008, ISO 22716/GMP and ISO 13485.
Solupharm Pharmarzeutische Erzeugnisse GmbH, a family business characterized by experience and competency, has been committed to the contract manufacturing of injection solutions and infusion solutions for more than 40 years.
Our name of Solupharm has been synonymous with high-quality, responsible contract manufacturing of sterile preparations in glass ampoules and glass phials. Our new building in Melsungen is one of the most modern production facilities in Germany.
Solvias is a world leader in contract research, development and manufacturing. The industries we serve include pharmaceuticals, biotech, medical devices and cosmetics. Solvias is a management- and employee-owned company headquartered near Basel, Switzerland. Our team of over 500 highly-qualified employees work closely together to find solutions that fulfill your requirements. We take pride in delivering the best quality and results for our customers. Our excellent infrastructure and unrivalled expertise ensure you can rely on us to move your substances and products forward. With a well-established scientific experience and proven track record, we provide integrated services, products and technologies to enhance the value chain for customers worldwide. Our service portfolio covers:
- Analytical Services
- Small Molecule Analysis
- Biopharmaceutical Analysis
- Solid-State Development
- Microbiology & Biological Analysis
- Ligands & Catalyst Technology
- Custom Synthesis & Manufacturing
Vioser S.A. is a dynamic and constantly expanding Greek pharmaceutical industry, established in 1984 in Trikala, Greece.Working strictly under the GMP regulations we can assure high quality, safety and reliability for our products and services. Our portfolio includes pharmaceutical I.V. solutions, generic antibiotics and CE marked irrigation solutions, bottled in polyethylene containers, produced with the Blow/Fill/Seal Technology®.
Since 1949, WALTER KREBS has been a specialized pharmaceutical wholesaler purchasing medication from around the world, for import and export purposes. A middle-sized company that stands out with an international network which has grown immensely over the decades. Combined with an extensive know-how of the customs and drug law governing regulations, end-to-end supply chain and excellent service.
The Wasdell Group provides the pharmaceutical and
nutraceutical industries with solutions to a range of outsourcing requirements.
Established in 1971, with multiple sites
in the United Kingdom and employing over 600 people, the group offers an
impressive range of technical, manufacturing, packaging and
The Wasdell Group prides itself on delivering high quality, reliable, flexible and responsive services with unrivalled lead times.