GermanyStand No: 3H80
BioChem GmbH is an independent, specialized contract laboratory located in Karlsruhe, Germany offering high quality laboratory services and competence in all areas of analytical, microbiological and molecular biological testing for the pharmaceutical, chemical, medical and cosmetics industry. The area of expertise covers not only Quality Control Release Testing or Analytical Development Activities, EU-Reanalysis or ICH-Stability Testing of raw materials or finished products of all dosage forms but additionally allows BioChem GmbH to handle cytostatics and narcotics. More than 70 experts at BioChem GmbH continuously offer competent solutions for your projects. BioChem GmbH is GMP-/GLP-certified as well as FDA-inspected and registered.
PortugalStand No: 3H100
FranceStand No: 3H82
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 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 their drug development pathway.
GermanyStand No: 3G76
Global BioPharma Product Testing within your reach As the largest international network of harmonized GMP and GLP product testing labs, Eurofins BioPharma Product Testing delivers a true local service experience. Eurofins BioPharma Product Testing offers the most complete range of testing services, harmonized quality systems to more than 800 virtual and large pharmaceutical, biopharmaceutical and medical device companies worldwide. In Our World, Global Is Local Our local presence ensures personal service backed by a unique global breadth of harmonized capabilities that support all functional areas of bio/pharmaceutical drug development and manufacturing, including method development, microbiology, process validation and quality control. With a global capacity of more than 92,000 square meters and facilities located in Australia, Belgium, Canada, Denmark, France, Germany, India, Ireland, Italy, Spain, Sweden, Switzerland, Netherlands, New Zealand, UK and the US, our network of GMP laboratories operates under the same strict quality procedures, LIMS and centralized billing system...
FranceStand No: 3F73
Europhartech, a contract manufacturing and development organization, has been recognized by pharmaceutical (human and veterinarian) and food supplements industries, for the adaptability of its services and the mastery of its supply chain. Thanks to high performing equipment, with continuous developments, Europhartech manufactures, in a fullservice approach, solid dosage forms for oral use (princeps, hormones, hospital, unit dose, probiotics, generics and food supplements). Uncoated, film/sugar/coated, flash tablets, hard gelatin capsules, and plant extracts drying with microwave technology. Blisters packaging (PVC, multilayers/alu, alu/alu) pots filling with counting control. Europhartech also offers development services, including production of pilot batches, stabilities studies until the industrial transposition.
GermanyStand No: 3G101
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.
FranceStand No: 3G91
Le Groupe CARSO, prestataire de référence depuis 25 ans, réalise des analyses et expertises dédiées à l'industrie des produits de santé: pharmaceutique, cosmétique et nutraceutique. Un service de proximité en analyses microbiologiques et physico-chimiques doté d'une plateforme analytique performante ICP-MS, MALDI-TOF, HPLC, GC. Autorisation d'ouverture d'un établissement pharmaceutique fabricant limité au contrôle de la qualité, délivrée par l'ANSM, décision n°F17/134 en date du 8 juin 2017. For 25 years, CARSO Group has been carrying out testing and expertise dedicated to the health industry: pharmaceutics, cosmetics and nutraceuticals. A convenience service in microbiology and chemistry testing equipped with an efficient analytical platform such as ICP-MS, MALDI –TOF, HPLC, GC; Authorization to open a pharmaceutical plant limited to quality control, issued by the ANSM, Decision No. F17 / 134 dated 8 June 2017.
SpainStand No: 3H72
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.
United KingdomStand No: 3H90
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...
ItalyStand No: 3H76
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.
United KingdomStand No: 3H71
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 and molecular biology.
ItalyStand No: 3G93
Neotron SpA is a global provider of analytical and testing services for pharmaceuticals, food, food supplements and ingredients, babyfood, packaging and cosmetics products. Neotron SpA, located in Italy, relies on a staff of more than 500 technicians skilled in analytical testing services and operating in a 10.000 m2 laboratory. Our great knowledge and the application of the most sensitive analytical techniques guarantee the highest level of reliability and performances. The laboratory is accredited according to ISO 17025, GMP certified and FDA approved.
FranceStand No: 3H101
GreeceStand No: 3G75
Established in the year 2002, the QACS Laboratory is based in Athens Greece, providing Quality Assurance & Quality Control Services to the consumer products industry for food and non food products, Cosmetics, Biocides, Pharmaceuticals, Foodstuffs. QACS operates in 600m2 premises, designed for and dedicated to testing activities. The company's core business is structured around the poles of Microbiology, Chemistry and Regulatory. Services include Regulatory and quality assurance (Safety Assessment, PIF-CPNP, GMP Compliance) supported by specialised laboratory services (Challenge Testing, Microbiological Enumeration, Traces Impurities, Patch Test, Stability Test). The QACS Laboratory is accredited by ESYD under the EN ISO 17025 standard for the testing of Foodstuffs & Cosmetics (certificate no 195), certified by Bureau Veritas under ISO 9001 and GLP compliant, certified by the National Organisation for Medicines (EOF) for performing chemical and microbiological tests on Cosmetics and Pharmaceuticals. The internal quality control scheme includes regular participation in inter-laboratory schemes. Founding...
BelgiumStand No: 3H104
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...
IndiaStand No: 3H94
SpainStand No: 3G72
Sincrofarm is a Contract Manufacturing Company of Medicines and Nutraceutical products for the pharmaceutical and healthcare industries. In medicine, we are specialise in hard capsules, tablets, coated tablets and powder. Sincrofarm can offer development, manufacturing, analysis, packaging and logistic services, Analysis, development and Stability studies
SpainStand No: 3H74
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
GermanyStand No: 3H81
Tentamus offers clients an international network of specialized laboratories with GMP, GLP and/or ISO accreditation. Even though the laboratories continue to operate under their original brands, they are all companies that are part of the Tentamus Group and are characterized by a high degree of integration, enabling us to optimally leverage the synergy of the individual laboratories.The Tentamus Group was founded early in 2011. Our goal was to become a well-respected provider of quality services and to ensure the continued quality and safety of our clients' products and services. We are proud to have quickly gained our customers' trust. We are represented in over 40 locations worldwide. More than 1,800 highly-trained staff members work in about a million square feet of laboratory and office spaces. This is how we apply our expertise and guarantee our clients the highest degree of reliability and quality. Representatives of different Tentamus laboratories like Analyst,...
GermanyStand No: 3H92
Developed with in-depth pharmaceutical industry experience, Thermo Scientific handheld analyzers provide manufacturers with a portable solution to achieve quality initiatives throughout the manufacturing process. The Thermo Scientific TruScan RM, based on Raman spectroscopy, and the Thermo Scientific microPHAZIR RX, based on Near-Infrared spectroscopy, enable on-the-spot, actionable Pass-Fail results within seconds.