Exhibitors

GB United Kingdom
Stand No: 41C40
About Almac Group ‘Partnering to Advance Human Health' The Almac Group is an established contract development and manufacturing organisation that provides an extensive range of integrated services to the pharmaceutical and biotech sectors globally. The services range from R&D, biomarker discovery and development, API manufacture, formulation development, clinical trial supply, IXRS® technology (IVRS/IWRS) through to commercial-scale manufacture. The international company is a privately owned organisation that has organically grown for 50 years and now employs in excess of 5,000 highly skilled personnel. Almac is headquartered in Craigavon, Northern Ireland with operations in the UK, Ireland, across the US (Pennsylvania, North Carolina and California) and in Asia (Singapore and Tokyo).
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NL Netherlands
Stand No: 41N14
New
Avivia is an independent specialized pharmaceutical development company engaged in drug repositioning, repurposing and reformulation. Our expertise and capabilities are centered around the development of value-added generic drugs, life cycle management of branded drug products, and complex formulation and CMC development of new drug products (NCE). We operate a hybrid business model combining CRO service activities with internal product development programs, whereby in both cases, we approach ‘development' as not just offering a technical solution but always part of a broader product-oriented strategy.
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Beijing Global Biologicals Co Ltd (GBC) is a biotechnology-driven company specialized in R&D and manufacturing of pharmaceutical ingredients and has two big manufacturing bases in Shandong of China. GBC provides the professional integration services of technology transfer, strain improvement, process optimization, research(CRO) and contract manufacturing (CMO) for APIs, intermediates, nutraceuticals, enzymes and agrochemicals. Our products include: Virginamycin,Avilamycin,Nicergoline,Astaxanthin,Glutathione (GSH), Mupirocin, Fusidic acid, UDCA,Milbemycin, Pneumocandin B0, Acarbose, G418 sulphate, Ergothioneine, Pyrroloquinoline quinone (PQQ),etc . Our Strains and Biotechnologies include:- strain improvement, biofermentation, biotransformation, enzymatic, DSP and purification, semi-chemical synthesis, scale-up, technology transfer,engineering consulting. Welcome to visit us web:http://en.globalbiologicals.com/
Location:
Sub-event: CPHI
Pavilion: China Pavilion
Biophore, an established pharmaceutical company is engaged in the development and manufacture of niche pharmaceutical products for generic industry.Within a decade since inception in 2007, Biophore has emerged as a trusted partner in generic industry across US, Europe and other regulated markets. Biophore's product range is diverse and balanced with NCE, Branded products and grandfather products. Biophore's portfolio spread across 30 therapeutic segments, is specialized in development and manufacture of pharmaceutical actives for Oncology medications, Contrast and Diagnostic media. For updated list of products, send an email to info@biophore.com
Location:
Sub-event: CPHI
Zone: API
US United States
Stand No: 80F92
New
BioSpectra – Booth 80F92: Your Premier Partner for US-Manufactured Life-Science Chemicals, Regulatory Compliance & Product Development – Your “Bespoke” Life Science Partner: BioSpectra is the premier US-Manufacturer of Life Science Actives, Intermediates, Excipients, Biological Buffers and Custom Products. FDA registered and inspected, we operate under true, US-GMP, IPEC and ICHQ-7 requirements out of 175,000 square feet of state-of-the-art facilities only 2-hours from NYC in historic Pennsylvania. BioSpectra stands apart as the only manufacturer of these products in the USA operating under these rigorous quality standards. Our comprehensive Total-Quality-System and Regulatory Support Services exceeds any other competitor, anywhere in the world, for the products we provide. Core Products: · Actives: KBr, KCl, NaCl, Tromethamine, Urea, & Custom APIs/ Oral, Transdermal & FUISA (For Use In Sterile Applications). · Excipients & Intermediates: Tromethamine, Guanidine HCl & Thiocyanate, HEPES, L-Cystine HCl, MOPS, Sugars (Galactose, Sucrose, Trehalose), TRIS HCl, Uracil, Urea, Ammonium Sulfate ·...
Location:
Sub-event: CPHI
Zone: API
CH Switzerland
Stand No: 110F30
Biosynth is a manufacturer and distributor of organic fine chemicals in the field of enzyme substrates, indole derivatives and speciality chemicals for microbiology, molecular biology, diagnostics, pharmaceutical industry, chemical industry, food and environmental testing.
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BR Brazil
Stand No: 61C40
Blanver is a Brazilian multinational company with more than 30 years of experience, 3 plants in Brazil and offices in the U.S. and Spain, which develops, manufactures and markets Finished Dosage Forms (FDFs) and pharmaceutical raw materials. Our pharmaceutical business plan is to export our FDF portfolio in the HIV and HCV segment, from Brazil through strategic and meaningful partnerships. We are seeking strategic alliances with international partners of recognized quality to license and commercialize innovative and established products in segments such as Oncology and Hematology throughout Brazil and Latin America. Become our partner, contact us for more information. +55 11 4138-8200 | contatobr@blanver.com.br
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Sub-event: CPHI
IT Italy
Stand No: 41A23
New
Capua 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...
Location:
Sub-event: ICSE
Zone: NEP ICSE
GB United Kingdom
Stand No: 61D32
Established in 2011, CMAC is a world-class international centre for manufacturing research and training. Working in partnership with industry, its purpose is to transform current manufacturing processes into the medicine supply chain of the future. The approaches developed and adopted within CMAC have been established through close collaboration with industry and the support of its partners, which include GlaxoSmithKline, AstraZeneca, Novartis, Bayer, Roche, Lilly and Takeda. The CMAC National Facility offers contract research support to industries through the delivery of services within crystallisation (batch & continuous), process development, formulation, product/process analysis and advanced materials characterisation. We are working with a range of companies based within the chemicals, agrichemicals and food industries applying our expertise in crystallisation, PAT and high end analytical services to these fields.
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Sub-event: CPHI
GB United Kingdom
Stand No: 41M02
Contract Manufacturing Excellence with Cobra Biologics Cobra Biologics is a leading international contract development and manufacturing organisation (CDMO) providing a comprehensive biologics and pharmaceuticals service offering. Our multi-functional and experienced project teams nurture customers' products through to clinical and commercial manufacture within three GMP approved facilities. Expertise Cobra is a contract development and manufacturing organisation (CDMO) supporting the global life sciences industry in the development and manufacture of monoclonal antibodies (mAb), recombinant proteins, DNA, viruses, phage and cell line derived products and pharmaceuticals for clinical trials and commercial supply. For Gene Therapy products we can produce DNA, Adenovirus, AAV, Lentivirus and other virus material for both clinical and commercial supply. Cobra provides manufacturing technologies, platforms and solutions for gene therapy products. For our AAV and Lentivirus customers we have developed a High Quality DNA platform process to enable the rapid supply of small quantities of DNA material for the production...
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US United States
Stand No: 111F53
Codexis is a leading protein engineering company applying innovative technologies to Unlock the Power of ProteinsTM. We work collaboratively with our clients to advance protein optimization and production, enabling breakthrough developments in pharmaceuticals and fine chemicals, biotherapeutics, food & beverage, agriculture and other industries.
Location:
Sub-event: CPHI
Zone: API
DE Germany
Stand No: 40F40
Dr. R. Pfleger GmbH is a midsized pharmaceutical company in Bamberg, Germany. It was established in 1945 and is owned by the Doktor-Robert-Pfleger-Foundation which supports medical research and charitable and social causes. We provide a full range of services for the development, manufacture, analysis, storage and distribution of pharmaceuticals, dietary supplements and cosmetics. Drawing on our over 70 years of experience, we supply products to more than 40 countries worldwide. Latest news: Our new R&D area is designed like a manufacturing on a small scale. It is compliant with all GMP-requirements and equipped with modern facilities, like the brand-new capsule filler from Harro Höfliger. We cordially invite you to visit us at our stand 40F40.
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IN India
Stand No: 40G62
Electrolab, established in 1984, manufactures pharmaceutical testing equipment such as dissolution testers, disintegration testers, friability testers, tap density testers, bulk density testers, electromagnetic sieve shakers, tablet hardness testers, leak testers, peristaltic pumps etc. For more than 28 years, the company has developed solutions that use state-of-art technology along with patented designs to solve our clients' challenges, setting an example for commitment to excellence. The company has a well-trained production team supported by in-house software, hardware and CAD engineers. Along with its network of distributors, Electrolab provides validation, support and prompt after sales service to meet customers' needs across 70 countries.
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Sub-event: PMEC
Zone: PMEC
GB United Kingdom
Stand No: 61D32
EPP is a GLP compliant Contract Research Organisation (CRO) assisting pharmaceutical companies with pre-clinical environmental sciences testing. We ensure the smooth and efficient registration of your products by following OECD guidelines and can provide bespoke testing as required. We specialise in GLP complaint testing in the areas of: · Ecotoxicology; aquatic, marine and terrestrial · Environmental fate · Fish metabolism studies · Controlled substances · Storage stability · Physico-chemical testing · NMR EPP can additionally support your pharmaceutical registration and QC testing processes by providing custom synthesis of rare or unusual (non-commercially available) analytical reference standards of metabolites, impurities or degradants which are comprehensively certified to GLP compliant standards including by the use of GLP compliant NMR (both qualitative and quantitative).
Location:
Sub-event: CPHI
FR France
Stand No: 41L50
Eurofins Amatsigroup is a leading international Contract Development and Manufacturing Organization (CDMO), headquartered in France. Within Amatsigroup, we provide high-quality, customized and cost-effective drug development solutions, integrated under one roof, to small biotech and major (bio) pharmaceutical customers. Our innovative and flexible approach enables customers to speed up their drug development process, achieving key milestones in a timely manner. The company has three strategic pillars: Drug substance process development and manufacturing for biologics, Pharmaceutical analysis solutions: fit-for-purpose method developments and validations, stability studies and Quality Control (QC) Formulation development and manufacturing of sterile and non-sterile clinical or small commercial batches. Clients also benefit from complementary services such as in-life studies, bioanalysis and clinical trial supply (packaging & logistics). A broad scientific, technical and regulatory expertise, combined with proactive troubleshooting skills, are the key assets of the company. Our goal is to build a sustainable partnership with our customers to support...
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IT Italy
Stand No: 40G66
Famar Tec is the heir of the great Famar experience. Located in Bologna (Italy), the well-known “Packaging Valley”, Famar Tec has developed a wide know-how in the design and manufacture of automatic machines for blisters, trays, cartons and cases for pharmaceutical, nutraceutical and cosmetic applications.
Location:
Sub-event: PMEC
Zone: PMEC
DE Germany
Stand No: 40C35
GBA Pharma is a service provider for pharmaceutical companies and is supporting research & development as well as services in the commercial stage. Our success and opportunities is based on a high qualified staff. The headcount of GBA Pharma represents 200 employees distributed over 5 locations in Europe with +50% academic staff. Our portfolio comprises the following service areas: Contract research in the preclinical arena (in vitro & in vivo) Pharmaceutical testing under GMP incl. stability study services & QP release services Bioanalysis under GLP: in vivo toxicology studies and phase-I/II clinical studies GMP qualification of API and drug manufacturer outside the European Union Distribution and clinical trial supply management for multicentre trials Consultancy & regulatory affairs with regard to GMP, GLP & GCP We would be delighted to develop a tailored solution for you.
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GB United Kingdom
Stand No: 92H79
Harmonium Pharma is a multinational company based in London, focused only on diabetes, which provides products and solutions for the daily management of this disease.Differently from other players focused on the management of hyperglycemia and on medical instruments (insulin, hypoglycemic, glucometers, strips, needles, insulin pumps), Harmonium Pharma provides a range of products which help day-by-day people with diabetes to manage aspects such as hypoglycemia, lipodystrophy, foot care, fingertips care, need of low glycemic index foods and prevention of complications such as neuropathy and retinopathy.
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Meishen Technology Co., Ltd. is a professional manufacture of magnesium oxide, magnesium carbonate, magnesium sulfate for food and pharmaceutical applications. Meishen is established in September, 2003, and now it is developed a group company owns 3 professional plants produce magnesium commodities and specialties for diversified industries and several famous brands like MeiShen, XingMei and MeiTai. Meishen Technology Co., Ltd is the leader of both manufacture and market of Magnesium chemical industry in China, and well recognized by the customers all around the world.
Location:
Sub-event: CPHI
Zone: API
Pavilion: China Pavilion
BR Brazil
Stand No: 110A41
ICF has been founded in 2002 and it has been the first Brazilian bioequivalence and bioavailability laboratory to get certified by ANVISA (Brazil). It is one of the largest pharmaceutical research centers in Brazil and in Latin America and a notable reference for industries and investors from several countries. ICF's commitment with ethics and innovation assure the credibility and quality of our products. ICF has already conducted over 700 bioequivalence studies and it takes part in the history of generic drugs in Brazil. We offer one of the biggest hospital infrastructures in the country with a high technology, diversified portfolio and certificate, two hundred bioanalytical methods – including high complexity methods such as hormones and sprays.?
Location:
Sub-event: CPHI
Zone: API
NL Netherlands
Stand No: 42N51
New
Who we are As a medical company, you may have a great idea for a device that will give you a competitive edge. But first you have to find a way to manufacture it according to the strict regulatory requirements for medical devices. IGS GeboJagema can help. For over 70 years, we have been delivering high precision moulds for some of the most successful metered dose inhalers, insulin pens, diagnostic products and other medical devices in the world. Many of the key players in the medical industry bring their toughest product challenges to IGS GeboJagema. That's because we provide the solutions they need to help them innovate new products. Our problem-solving mindset, proven track record in the healthcare industry, considerable medical experience and meticulously methodical way of working ensures you the highest quality, process control and traceability needed for your medical products. We make moulds for products you still have...
Location:
Sub-event: InnoPack
Zone: InnoPack
ES Spain
Stand No: 41A51
InKemia generates high technological knowledge to give support to the life science industry through its business lines: co-development, contract research, licensing-out, technological services, competitive R&D grant programs, technical and quality consultancy and training. InKemia's core competencies are chemical synthesis, analytical development, impurity studies, biotechnology and bio-catalysis, quality control and EU release.
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GB United Kingdom
Stand No: 40F33
Helping our clients achieve Total Quality Assurance through custom, flexible, contract services from a single source, our scientists, auditors and regulatory experts work with you at every stage of development, providing GMP and CMC Laboratory Services, GMP Auditing, GLP/GCP Bioanalysis, Regulatory and Toxicology Consulting and Pharmaceutical Manufacturing Support. Our Good Laboratory Practice (GLP) and Good Manufacturing Practice (cGMP) laboratory network have provided high quality technical services for some of the world's largest and most innovative pharmaceutical companies. GMP and CMC Laboratory Services We provide regulatory-driven, phase-appropriate laboratory services in support of CMC programs seeing you through preformulation, formulation and product release. Our capabilities include centres of excellence for method development and validation, analysis, stability studies, extractables and leachables, solid state characterisation, cGMP quality control testing and cGMP batch release testing. Our teams have specialist expertise for complex medicines and drug delivery systems such as inhalation drug product development for pulmonary...
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IT Italy
Stand No: 40K57
New
Since it was founded in 1991, IWT has been a pioneer in the design, development and industrialization of industry standard automated washing equipment. Our engineering embraces advance techniques encompassing: - Fully validated processes inclusive of critical parameters monitoring and tracking - Complete prevention of cross contamination - Improved operators' safety - High throughput resulting in minimal production downtime IWT solutions include full cGMP products contact part washers, as well as high pressure washing systems either for bulk containers in Cleaning-In-Place applications or cabins for bulk parts and containers Cleaning-Out-Of-Place. Our experience in cleaning, combined with proven specific skills and know-how, are at your disposal to define together the most suitable and efficient solution inclusive of related services (calibration, qualification and validation) to meet your specific needs.
Location:
Sub-event: PMEC
Zone: PMEC
ES Spain
Stand No: 91B30
Kymos is a reliable CRO, certified in GLP and GMP with laboratories in Spain and Italy. Kymos provides contract research, development and analytical services for pharmaceutical, biotechnology, veterinary, fine chemistry, cosmetics and nutraceuticals industries. The main areas of activity are: i) batch testing, batch release and importing of medicinal drug products for human, veterinary and investigational use in the EU; ii) quality control of raw materials and finished drug products, analytical development and validation, stability studies, microbiological testing and PAT-QbD consultancy; iii) biopharmaceutical testing of proteins an monoclonal antibodies and comparability of biosimilars; iv) immunogenicity testing, cell based assays and bioanalysis of biologics and small molecules, including full management o bioequivalence studies.
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The Spark-Lab company, a research and development laboratory built exclusively on Polish capital, was created in 2010 and has been rapidly expanding ever since. Our team of executives consists of scientists affiliated with leading academic institutions in the Tricity area (Gdansk University of Technology, Medical University of Gdansk). The ever increasing demands towards production companies belonging to various branches of industry force a great amount of qualitative and quantitative standards for their products. Production process itself generates numerous problems on its various stages. Establishing internal research and developmnet departments requires vast financial resources to be invested in the purchase of measurement equipment as well as employment of highly qualified personnel. In an attempt to meet the growing needs of pharmaceutical, chemical and cosmetic sectors, Spark-Lab offers research and development services along with various routine analyses, thus serving as an external laboratory for your company. High-end measuring devices allow us to...
Location:
Sub-event: CPHI
GB United Kingdom
Stand No: 40D35
LGC is an international life sciences measurement and testing company. Operating from state-of-the-art facilities to GLP, GCP and cGMP standards, LGC has leading capabilities in CMC, with particular specialties in materials science and pharmaceutical analysis. In support of the development and manufacturing of small and large molecule drugs, LGC provides method development, ICH validation and routine testing services. We offer unknown impurity determination, structure elucidation, compatibility studies, stability storage and testing. We are a leading provider of extractables and leachables studies and elemental impurity analysis. Our World-class material characterisation capability supports formulation development and manufacturing. LGC also has a state of the art bioanalytical capability in high-integrity analytical science and expertise spanning small and large molecules, biomarkers, molecular biology and microbiology.
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CH Switzerland
Stand No: 42N53
New
Lonstroff, a Swiss company specialising in the production of rubber components, developed in 1993 an innovative production line of pharmaceutical and medical rubber parts (including coated and silicone free solutions) that has received an outstanding reputation in the international pharma industry. Since 2015 Lonstroff belongs to Sumitomo Rubber Industries.
Location:
Sub-event: InnoPack
Zone: InnoPack
Medecell Group is a company with 20 years experience; we've been a leader in providing the global markets with the best in new product development, international commerce and consulting services. Medecell is a company which has been solely dedicated in bring the best in cutting edge consumer related technologies and in exclusive health care products.
Location:
Sub-event: CPHI
Zone: API
FR France
Stand No: 41A10
New
Medelpharm is a high-precision engineering company manufacturing research and development (R&D) tableting instruments and providing innovative solutions for powder analysis and formulation. The company focuses on continuous development of innovative research presses, mimicking industrial production cycles, powder characterisation and formulation services for the pharmaceutical, food and cosmetics markets.
Location:
Sub-event: ICSE
Zone: NEP ICSE
IT Italy
Stand No: 42M54
Since the 1980s, Metalco-Alupack manufactures aluminium primary packaging for sterile APIs and other sensitive products. Metalco-Alupack has registered a Type III (packaging) DMF with the USFDA which is updated and enriched annually. Anodised canisters ensure perfect chemical stability, complete protection and efficient tightness. They are easy to sterilize and depyrogenise. Our canisters can be conveniently sterilised, after washing and rinsing, using dry heat sterilisation or autoclaving; they are even found to be pyrogen free, when tested. Seamless aluminium containers are indeed completely neutral either from a mechanical point of view (they are resistant to schocks, perforation, cuts, etc..) or from a chemical one ( Alu canisters give absolute protection to cold and heat, light and gas permeation, etc..) Metalco-Alupack has worked in partnership with the mayor pharmaceutical users to increase the final surface treatment of alu cans for sterile powders. We guarantee the level of cleanliness according to the most...
Location:
Sub-event: InnoPack
Zone: InnoPack
Your North American Specialty Pharmaceutical Partner Methapharm is a privately held specialty pharmaceutical company with a focus on the acquisition, licensing, and promotion of healthcare products in North America. We market our own proprietary products as well as partner with global companies to deliver a comprehensive line of specialty products in the USA and Canada. As an integrated specialty products company, we offer our partners sales and marketing, distribution, market access, regulatory, quality, medical, and pharmacovigilance capabilities in North America. We are part of the ACIC group of companies which operate in the fields of API and finished product development, manufacturing, and supply. Come visit us at CPhI - or contact us to make an appointment.
Location:
Sub-event: CPHI
Zone: API
DE Germany
Stand No: 40G70
NARA offers special machines and devices for powder and particle processing, creation and optimization of particle quality, e.g. in the pharmaceutical and chemical industry. The main product range includes dryers, milling and powder design (well-aimed modification of particle surface).
Location:
Sub-event: PMEC
Zone: PMEC
AT Austria
Stand No: 41G30
Ortner is an Austrian-based manufacturer and system provider of standardized and bespoke equipment and solutions for all kinds of cleanroom requirements within the research and life science market. Over the last 30 years, Ortner has built up a wealth of expertise and knowledge in cleanroom technology and has proven R&D capabilities in barrier, containment and decontamination solutionsfor fast, safe and reliable protection of people, animals, research and the environment against contaminants and particles.
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Pharmaffiliates Analytics & Synthetics (P) Ltd, is an integrated CRO (Contract Reserach Organisition) established in year 2005. Presently we are US-FDA accredited Facility We are specialized in research via synthesis of complex and difficult to make compounds, innovative organic molecules to support and accelerate the drug discovery research of pharma and biotech companies. We adapt unique synthetic approaches and execute in robust ways for making complex and unknown impurities with their characterization data. Thus we make the drug discovery process more efficient, cost-effective while maintaining the highest standards of quality. With the collective efforts of our team of 130 scientists so, far, we have performed more than 300 method validations & many of these validation reports submitted to EU & US & sought approvals. Work is carried in line with the ICH and the GMP guidance. Our experience, combined with state-of- the-art laboratories and manufacturing facilities lets us become an...
Location:
Sub-event: CPHI
DE Germany
Stand No: 40L60
New
PINK GmbH Thermosysteme – founded by Friedrich Pink – is located in Wertheim and employs a workforce of over 100 employees. Its versatile and all-embracing product range includes plants for drying and processing technology, systems for vacuum-supported soldering, sintering systems as well as low-pressure plasma plants. PINK operates in all major markets and supplies individual plants and systems all over the world. These enjoy an excellent reputation in terms of design, reliability, performance, user comfort and quality. Well-known technology companies rely on the company's innovative and high-quality products. Due to continuous product improvements and a consequent customer orientation in the past years, the PINK family business has grown steadily and successfully and has become a byword for vacuum, drying and processing equipment. Its extensive product range in the drying sector extends from static dryers in various designs, sizes and equipment versions through to dynamic drying systems working on different drying...
Location:
Sub-event: PMEC
Zone: PMEC
IT Italy
Stand No: 40B40
Since 2005 PolyCrystalline provides reliable solutions to optimise and control the crystallisation process of Active Pharmaceutical Ingredients for pharmaceutical companies. Our mission is to support our clients during drug development, helping them to reduce batch failure, avoiding costly crystallisation issues and overall offering greater confidence in drug quality during manufacturing. We can support you from early-phase drug discovery to kilogram supply. We are a high performing cohesive team of trained chemists and analysts, with more than 10 years of experience in the development and optimization of APIs crystallization. We care about results and innovation based on sound science and the use of modern technologies.
Location:
BE Belgium
Stand No: 42C23
Quality Assistance SA is a leading European Contract Research Organisation providing the pharmaceutical industry with all the analytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products. Quality Assistance assists its clients from candidate selection, through non-clinical and clinical studies, to marketing authorisation, using state-of-the-art, product-dedicated expertise in analytical sciences. For each customer and each project, Quality Assistance designs customised solutions, define analytical protocols, develop and validate specific new analytical methods and perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing, in order to evaluate the Quality, Safety and Efficacy of the given drugs. Founded in 1982, the company holds a unique position on the market with 140 highly qualified professionals and all of its laboratories on one site: Bioanalysis (PK/TK/Immuno), bioassays, biochemistry, chromatography, Elemental Impurities, Mass Spectrometry, microbiology, molecular biology, protein characterisation. Quality Assistance is an...
Location:
IN India
Stand No: 91A76
We are dealing with high-quality Active Pharmaceutical Ingredients (APIs), Formulations, New Drug Delivery Systems and Specialty Chemicals utilising sophisticated technology meticulously in order to comply with international standards/specifications. Today we are among the world's leading suppliers of Oncology/non- Oncology APIs, intermediates and Formulations. Shilpa Medicare's facilities have received key regulatory approvals for its facilities as well as for the products from USFDA, EUGMP, TGA, PMDA, Cofepris, Anvisa and KFDA with diverse regulatory recognized manufacturing set ups and excellent scientific manpower. We are ISO 14001: 2004 certified organization and committed to implement, maintain and improve the environmental management system so as to assure its conformity with our stated environmental policy. We offer a broad and integrated portfolio of products and services (CRAMS) to the global pharmaceutical industry. Being proactive in approach, we continuously seek out avenues and first available opportunities for development of new products drawing strength from our zeal to...
Location:
BG Bulgaria
Stand No: 40K53
SoftGroup is an innovative IT company providing pharmaceutical manufacturers with complete serialisation solutions including hardware, software, implentation, validation, documentation and 24/7 support. Our SoftGroup® SaTT (Serialization and Track & Trace) is an integrated mass serialisation system for centralized management of pharmaceutical packaging lines covering Levels from 1 to 5.
Location:
Sub-event: PMEC
Zone: PMEC
BE Belgium
Stand No: 40K71
New
Systech, a global leader in product verification and brand protection, is re-defining the future of authentication. As the innovator of serialization, Systech is trusted by top pharmaceutical companies worldwide to ensure regulatory compliance, mitigate risk, ensure supply chain integrity, and drive efficiency. Beyond compliance, the company is leading the charge to protect global brands—for consumer packaged goods, food & beverage, health & beauty, pharmaceutical, and contract manufacturing companies. Its best practices and award-winning technologies are guiding Product and Brand Protection Officers in their quest to improve patient/consumer safety, increase engagement, decrease counterfeiting, avoid diversion, and reduce harm to coveted brands.
Location:
Sub-event: PMEC
Zone: PMEC
IN India
Stand No: 111D73SSP
TCG Lifesciences Pvt. Ltd. (formerly "Chembiotek") is a leading contract services company in the area of drug discovery, development, and manufacturing. Our operations opened in 2001 in India and comprise of three facilities located in Kolkata and Hyderabad. Our services span discovery through cGMP manufacturing including medicinal chemistry, in vitro and in vivo biology, process development, scale up, and cGMP manufacturing. Our team includes more than 700 qualified and trained scientists and technical staff, drawn from the best international institutions and industry. Our teams operate in two facilities in Kolkata comprised of 250,000 sq. ft. of world class chemistry and biology labs, a 10,000 sq. ft. animal facility, electrophysiology lab, BSL 2 lab, and cGMP facilities. We have expertise across multiple therapeutic areas with focus on Inflammation & Pain, Infectious Diseases and Central Nervous System (CNS). Our manufacturing facility in Hyderabad includes ~140,000 L of reactor capacity on a 7.5...
Location:
Sub-event: CPHI
Zone: API
DE Germany
Stand No: 40A23
New
Testo industrial services GmbH is a leading service provider company in the field of calibration, qualification, validation as well as test equipment management. Worldwide unique are the laboratories which are accredited for more than 190 calibration procedures.
Location:
BE Belgium
Stand No: 42C31
Toxikon is a preclinical CRO with ISO, GMP and GLP accreditations in the USA and Europe. Both laboratories are registered with FDA and provide over 30 years of experience in product development services. We support pharma, biotech and medical device industries to deliver exceptional product development services from concept to final product. With our in vivo capabilities ranging from mice to non-human primates, we can provide early proof-of-concept studies and full GLP toxicology studies to support your IND/NDA submission. With analytical services for impurities, bio-analytics up to stability testing and microbiology. At Toxikon, we take time to design your project.
Location:
AT Austria
Stand No: 41G30
VTU Engineering is engineer, GMP consultant and supplier for the pharmaceutical, life science and biotech industries. We offer the highest expertise in all project phases from feasibility, project management, basic and detail engineering up to a successful start-up of process plants. The bandwidth of the technologies being used ranges from active pharmaceutical ingredient production (API), continues with biotechnology with different hosts and complex requirements in downstream processing (also for products from blood), up to a great variety of galenic productions. Auxiliary systems like, for example, ultra-pure media, CIP, clean rooms as well as control and data capture systems also have special requirements. coolox® Wastewater Treatment is a new combination of processes to clean wastewaters without employing vast amounts of chemicals – and thus cost-effectively and environmentally benign. Highly Active and/or Persistent organic pollutants in water are fully decomposed. Individually tailored solutions operate fully automated and require low operating costs as...
Location:
AT Austria
Stand No: 41G30
Pichia pastoris Protein Expression / Production Excellence Be competitive with high-quality proteins, high-productivity strains & robust and scalable bioprocesses from world´s broadest Pichia pastoris protein production toolbox VTU Technology is a leading contract research and development company, providing time-saving development of cost-efficient recombinant protein production processes for manufacturing of biologics and other proteins Cutting-edge, exclusive, proprietary technologies and extensive know-how are the basis for the broadest toolbox and most versatile technology platform available for Pichia pastoris recombinant protein expression / production enabling highest productivities of up to 25 g/L of secreted protein (peak productivity of 35 g/L) for e.g. cytokines, growth factors, hormones, serum proteins to fusion proteins (Fc-and albumin fusion), protein scaffolds, antibody fragments and vaccine antigens, enzymes or allergens. VTU guarantees tight development timelines and competitive & safe production processes. Unlock Pichia - VTU Technology´s toolbox: Exclusive AOX1 promoter libraries Diverse set of platform strains Proprietary expression enhancing...
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Established in the year 1965, 'West Coast Pharmaceutical Works Limited' has garnered a respectable name for itself in the domain of processing, supplying and exporting pharmaceutical products. Over the years, we have grown into a vast organization. Our experience and dedication makes us capable of processing all kinds of effective medicinal products. We are Manufacturer of Pharmaceutical Products for various categories of products • Anti-Cancer Tablet & Capsule. • Hormones Tablet & Capsule. • ?-Lactum Table. (Coated / Uncoated). • ?-Lactum Capsule & Dry Syrup. • Oral Powder (ORS, PROTEIN POWDER,) • Oral Liquid Section. • General Tablet & Capsule. • Disinfectant Products. (All hospital disinfectant products) • External Liquid/Ointment/Gel/Lotion/Nasal spray • Cosmetics products.(CREAM/ GEL/ LOTION/SOAPS/SHAMPOO/OILS) • Medicated Soaps • General Powder Repacking. • Liquid Repacking. • Dietary Supplement/Food Supplements/Nutraceutical products. We are also manufacturing following category of products. • Cosmeceutical Products (Medicated Cosmetics Mfg. Under Cosmetic Lic) • Veterinary...
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JP Japan
Stand No: 80A72
Yamasa was founded in 1645 as a manufacturer of soy sauce. During 372 years of company history, we have dedicated our effort to make quality our top priority. Although Yamasa is now known worldwide as a leading soy sauce company, Yamasa raised another ideal in 1976, by declaring our commitment to the life industry. Since then Yamasa has played an important role in sustaining research and industrialization of nucleic acids. In the field of nucleic acids, Yamasa has the reputation of top class company in the world for the supply capability, the productive technique, and the quality management.
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Sub-event: CPHI
Zone: API