Exhibitors

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.
Location:
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.
Location:
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.
Location:
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...
Location:
DE Germany
Stand No: 110F30
Explicat supports, advises and assists pharmaceutical companies, manufacturers, developers and laboratories around the world. Our broad range of services include: Technical Project Management Pharmaceutical Development Medical Device Development Formulation Development Technical Due Diligence Qualified Person Services Process Analytical Technology (PAT) Quality by Design Development
Location:
FR France
Stand No: 41F70
galien+ is a new CDMO with 3 sites, located in Burgundy, France @ Auxerre Site is offering a wide range of manufacturing capabilities, with a strong focus on solid doses, powder sachet filling and a dedicated high potent drugs facility. @Nevers, Site is specialized in LYOC - Lyophilized freeze dried tablets (ODT). @ Sens, Site is offering capacities in Blister Packaging, QC, Stability Studies, and a wide range of pharmaceutical services from Analytical Development & validation to Graphic Art services, Scientific and Regulatory services.
Location:
CH Switzerland
Stand No: 61B30
Ginsana SA (trading as SFI Switzerland) is part of SFI Group and offers natural clinically proven branded products distributed worldwide. Ginsana SA is also a reliable service provider for Product Development, Regulatory Affairs, Manufacturing, Packaging and Analytics. Ginsana SA's manufacturing site is approved by Swissmedic, ANVISA and Saudi FDA
Location:
Sub-event: CPHI
DE Germany
Stand No: 40A20
HENNIG Arzneimittel is a mid-sized family-owned German pharmaceutical company based near Frankfurt with almost 120 years of grown experience. Its success is based upon four main pillars : HENNIG Arzneimittel offers proprietary drugs to the German market in the indication vertigo and disturbances of equilibrium where it is market leader. Besides this HENNIG Arzneimittel manufactures and offers a broad range of generics - among these all generically available antivertigo products. Further core areas regard cardiovascular, metabolism, pain, neurologic and psychiatric products. A rapidly growing range of over-the-counter drugs, devices and food supplements is complementing HENNIG's product portfolio, strengthening its consumer orientation. The fourth pillar is contract manufacturing and contract development services, both for pharmaceuticals and food supplements, with a special focus upon complex solid dosage forms for modified release. Technologies include tableting, coating, dry and wet granulation, extrusion, pelletising, dry-coated tablets and capsule filling, as well as blistering and secondary...
Location:
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.
Location:
DE Germany
Stand No: 40D31
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...
Location:
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.
Location:
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...
Location:
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.
Location:
DE Germany
Stand No: 41A03
New
MJR PharmJet is a provider of formulation development and manufacturing services for pharmaceuticals with a special focus on the low soluble substances. We offer a broad range of particle types and technologies in order to meet your needs in enhanced bioavailability or stability, preventing fed/fasted state differences, taste and smell masking, ER or MR formulations. Services all around the particles: Development of nanoparticle systems for oral, parenteral, pulmonary or topical applications together with our partner leon-nanodrugs Development of encapsulation system for taste/smell masking Enhanced stability in liquid for RTU formulations Micro-particulate systems for extended release formulations Particle based drug delivery systems and drug targeting Particle technologies screening studies for NCEs together with our partner leon-nanodrugs Particles for in-vivo and in-vitro diagnostics Particle systems for medicinal product applications Furthermore, we provide technology transfer services for your established nanoparticle and microparticle formulations to increase the GMP compliance and efficiency of the production...
Location:
Sub-event: ICSE
Zone: NEP ICSE
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
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:
SE Sweden
Stand No: 41K10
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
Location:
ES Spain
Stand No: 90G76
Reig Jofre is a Spanish pharmaceutical company focused on the Research, Development, Manufacture and Marketing of pharmaceutical products and nutritional supplements, as well as on specialized contract development and manufacturing. Reig Jofre has 850 employees, 4 development and manufacturing centers in Europe, direct sales in 6 countries in Europe and over 130 commercial partners in 58 countries worldwide. The company reached sales of €157 M in 2015 and is #5 Spanish pharmaceutical company by turnover listed on the Spanish stock market. Reig Jofre's three product categories within RJF Pharma (79% of 2015 sales) are: i) technological-specialization products (i.e. beta-lactam antibiotics, injectable and freeze-dried products); ii) therapeutic-specialization products in the areas of dermatology, respiratory/ENT and gynecology; and iii) food supplements and consumer healthcare products. High technology standards and a sound track record in the above technological-specialization products have turned Reig Jofre as the chosen partner of many companies worldwide for their...
Location:
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
Location:
ES Spain
Stand No: 40D33
TECNALIA offers services and R&D across entire value chain(human medicines, medical devices, food supplements, cosmetics & veterinary medicines). • Pharmaceutical development:Galenic & Analytical Development, Analytical methods Validations, Stability Studies • Clinical Trials:Bioequivalence Studies, PhaseI,II,III&IV Clinical Trials, Nutritional Clinical Studies. • Manufacturing:Contract Manufacturing of Industrial Batches for Third Parties • Pharmacogenetics
Location:
FR France
Stand No: 40A51
Wyjolab SA is an advanced GMP-compliant pharmaceutical laboratory that works with leading healthcare companies to develop and manufacture pharmaceuticals and nutritional products. Wyjolab's state-of-the-art facilities offer customers a wide range of dosage forms (liquids, semi-liquids, powders, extruded polymer, etc.) and many packaging solutions including stick-packs. A strict quality control process guarantees quality from raw materials to finished product. Wyjolab is equipped to conduct constant tests throughout the development process or in ongoing test protocols. With nearly 30 years of experience in product development, Wyjolab also has deep expertise in galenic and analytical services, as well as suspension and oral applicator technologies.
Location: