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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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US United States
Stand No: 80G22
Albany Molecular Research Inc. (AMRI) is a global contract research and manufacturing organization that has been working with the Life Sciences industry to improve patient outcomes and the quality of life for more twenty-five years. With locations in North America, Europe and Asia, our key business segments include Discovery and Development Solutions (DDS), Active Pharmaceutical Ingredients (API), and Drug Product Manufacturing (DPM). Our DDS segment provides comprehensive services from hit identification to IND, including expertise with diverse chemistry, library design and synthesis, in vitro biology and pharmacology, drug metabolism and pharmacokinetics, as well as natural products. API supports the chemical development and cGMP manufacture of complex API, including potent, controlled substances, biologics, peptides, steroids, hormones, cytotoxic compounds and sterile API. DPM supports development through commercial scale production of complex liquid-filled and lyophilized parenterals, sterile suspensions and ophthalmic formulations.
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Sub-event: CPHI
Zone: API
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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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).
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Sub-event: CPHI
FR France
Stand No: 41D50
Holochem is a Contract Research Organization offering R&D services for the development of key intermediates and APIs. We produce pre-clinical batches from milligram to kilo-scale for early-phase formulation and toxicological use. Our custom synthesis services cover all phases of Chemical and Process development, from the design of an original synthesis pathway and the development of the industrial process, to the development and validation of the associated analytical methods. We have expertise in various advanced chemistry technologies and compounds including small and complex molecules, Highly Potent APIs, ADC linkers, impurities and metabolites. All key intermediates, active ingredients and reference substances developed by Holochem are fully EP/USP/ICH compliant and benefit from IMPD/IND/DMP regulatory support. As part of our integrated services we can assist our pharmaceutical customers with the drafting of their regulatory files. At Holochem we value close collaboration with our customers and open communication at all stages of the development process...
Location:
Sub-event: ICSE
Pavilion: France Pavilion
FR France
Stand No: 41D50
Holodiag is a Contract Research Organization offering R&D services dedicated to pharmaceutical solid state and crystallization process. ¤ Analytical characterizations : XRPD, DSC/TGA, DVS, polarimetry, FTIR/UV, pKa/logP/logD, KF, IDR. ¤ Solid state investigations : screenings (polymorphs, salts, co-crystals, amorphous), stability/solubility/dissolution. ¤ Crystallization process : development/optimization, product recovery, isomer separation, filtration.
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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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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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IT Italy
Stand No: 40F60
New
LabAnalysis offers its services to pharmaceutical companies by supporting them during routine quality control analysis as well as method development and validation procedures both in chemical and microbiological fields. Our laboratory is in compliance with GMP and it also has FDA approval. It has won the approval of Pharma Authorities since 1996 and thanks to its high quality system and laboratory facilities, its analytical activities and foreign business relationships are growing steadily year by year.
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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...
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Sub-event: CPHI
DE Germany
Stand No: 40D21
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, canisters, IBC bulk containers, tubes to stick packs. 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.
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AT Austria
Stand No: 41G30
Perception Park is a company passionate about Hyperspectral Imaging, Chemical Imaging and Chemical Colour Imaging. Perception Park's main focus is on generic and configurable processing solutions for industrial inline applications. Our systems are well established in pharmaceutical, food processing, recycling and mining industries. We are committed to delivering the highest performance, extendibility and compatibility. Our plugin concept means that new devices are quickly supported. This gives our customers freedom, independence and individuality in their development activities and opens up endless possibilities for new applications, while saving development time and money.
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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...
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Sub-event: CPHI
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...
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CH Switzerland
Stand No: 42B30
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.
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CN China
Stand No: 101B43NEP
New
Ninth Water is a China based, innovative company driven by our passion in techniques and insights into rising market needs. We create unique value to our customers by providing essential products and service with highest industrial standard. Biopharmaceutical, analytical and performance chemicals are our core markets. Our management team comes from most reputable chemical and pharm companies like Dow Chemical, Sinopec and J&J. We started our business from 2014 and supply high purity acetonitrile to pharmaceutical and analytical customers since then. We are No. 1 HPLC grade ACN manufacturer (3000t capacity) in China since then. Besides high purity solvents, we also provide HPLC solvents reuse equipment (with our partner CNOOC), bringing over 30% solvents saving for peptide purification. Ninth Water has strong interests in biopharmaceuticals. Besides supplying the consumables, we continuously invest on research projects specifically of regulation peptides that stimulate the vaccine immune response, along with professors from Fudan...
Location:
Sub-event: CPHI
Zone: API
CH Switzerland
Stand No: 40F41
Solvias is a world leader in contract research, development and manufacturing. The industries we serve include pharmaceuticals, biotech, medical devices, cosmetics, chemical, electronic materials, life sciences and oil. Solvias is a management- and employee-owned company headquartered near Basel, Switzerland. Our team of over 400 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
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GB United Kingdom
Stand No: 42A15
Source Bioscience is a leading independent, MHRA approved (cGMP) CRO that specialises in chemistry, manufacturing and control (CMC) laboratory services for all phases of drug development. Supporting the pharmaceutical research and development process from preclinical enabling studies, through the clinical research phases and batch release testing into the market place.
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