Exhibitors

US United States
Stand No: 40D34
B&W Tek is the global leader in innovative mobile spectroscopy solutions. We utilize our own key building blocks consisting of spectrometers, light sources, sampling accessories and software capabilities to produce portable and handheld spectroscopy and laser instrumentation. B&W Tek provides Raman, LIBS, UV-Vis and NIR solutions for the pharmaceutical, biomedical, physical, chemical, safety, security, research and education communities.
Sub-EventZoneStand No
40D34
DE Germany
Stand No: 40D32
Bioassay GmbH is an independent contract laboratory located in Heidelberg (Germany), specializing in the development, validation and routine performance of bioanalytical assays in the area of Pharmacology and Toxicology. We carry out qualified analytical services on the sound basis of our GMP & GLP certification, which provides an excellent framework for successful projects and routine bioanalysis.
Sub-EventZoneStand No
40D32
Categories:
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.
Sub-EventZoneStand No
40C30
IN India
Stand No: 40C32
Clearsynth is a technology based, research driven enterprise with the World's Largest Inventory of Reference Standards & Research Chemicals. We aim to enable the research community in accelerated discovery via synthesis of complex and difficult to make compounds. We specialize in Innovative Organic chemistry and synthesis of Unique Complex Molecules, Stable Isotope Labelled compounds, Metabolites, Impurities, Glucuronides, Chiral Compounds, Conjugate Impurities, and Radioactive Labelled Compounds. We also undertake synthesis of complex Molecules or "Difficult to Synthesize" compounds/Intermediates. Product Categories : Popular Categories : , Reference Standards, APIs, Stable Isotopes, Metabolites, Impurities, Glucuronides, Deuterated Solvents and Reagents, Chiral Standards Other Categories : Intermediates, Fine Chemicals, Phytochemicals, Catalysts, Inhibitors, Peptides, NMR Solvents, Amino Acid Derivatives, Fatty Acid Derivatives, Diagnostics, Environmental, Biochemicals, Steroids, Vitamins, Activators, Agonist, Anti-virals, Biotin Derivatives, Boron Derivatives, Carbohydrates, Chelating Agents and Ligands, Cyanine Dyes, Detergents, Maleimide Derivatives, Nitric Oxide Reagents, Neurochemicals, Nicotine Derivatives, Glycerols, NMR Solvents, Nucleotides, Oligosaccharides, Wittig...
Sub-EventZoneStand No
40C32
DE Germany
Stand No: 40D30
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 65,000 square meters and facilities located in Australia, Belgium, Canada, Denmark, France, Germany, Ireland, Italy, Spain, Sweden, Netherlands, UK and the US, our network of GMP laboratories operates under the same strict quality procedures, LIMS and centralized billing system across 25 locations worldwide...
Sub-EventZoneStand No
40D30
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.
Sub-EventZoneStand No
40C35
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...
Sub-EventZoneStand No
40D31
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...
Sub-EventZoneStand No
40F33
Categories:
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.
Sub-EventZoneStand No
40D35
IT Italy
Stand No: 40B36
Neotron is a global provider of analytical and testing services in the market of food, packaging, cosmetics, food supplements and pharma products. Neotron relies on over 400 members of staff dedicated to food safety and nutritional testing in 10.000sqm of laboratories located in Italy. Great knowledge of food chemistry and application of the most sensitive analytical techniques guarantee the highest level of reliability and performances. The lab is accredited according to ISO 17025 and GMP certified.
Sub-EventZoneStand No
40B36
AT Austria
Stand No: 40B32
OFI provides assistance for the targeted, efficient development of your new products. Your concerns will always be given priority. Why? Because, rather than developing our own products, we act as a 100% privately owned, independent and self funded research and testing institute. Whether medicines are in the development or authorisation stage, or already on the market, we offer you international services based on GMP, EMA and US guidelines and testing of primary, secondary and tertiary packaging materials.
Sub-EventZoneStand No
40B32
Panexcell is a well-established BA/BE centre at Mumbai, INDIA with total Bed Capacity of 58 and 21 CFR, Part 11 compliant sophisticated instruments like LCMS - API 5500. Panexcell have a comprehensive total quality management systems, standard processes specifically designed for high-quality deliverables, a sustained and reliable regulatory environment, and highly trained manpower. Services Offered in BA/BE: • Bio-Availability / Bio-Equivalence Studies • Pharmacokinetic Studies with NDDS and NCEs • Bio-analytical • Statistical Analysis • Data Management • Medical Writing • Special Population Studies Clinical Trials: • Proof of concept studies • Phase I - Phase IV Clinical studies • Disease prevalence and modality of the treatment • Safety monitoring • Pharmacovigilance • Therapeutic training Medical Writing: Our Medical writing team supports the planning and conduct of studies with utmost focus on safety. Their role comprises protocol designing, interacting with key operation leaders in specific therapeutic areas to obtain their...
Sub-EventZoneStand No
40C31
GR Greece
Stand No: 40C33
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...
Sub-EventZoneStand No
40C33
US United States
Stand No: 40C37
Transdermal. Transmucosal/Oral Film. Topical. Tapemark is a CDMO providing web-based (flexible roll goods) manufacturing for drug delivery including formulation, blending, coating, converting, packaging, laboratory services. Tapemark is a market leader in transdermal drug delivery, oral and transmucosal soluble film, and Tapemark's patented Snap!® and Snapplicator™ packaging supports unit-dose topical drug delivery. Tapemark is cGMP-compliant, ISO 9001 and 13485 certified, and FDA registered as a Drug, Device, Food, Cosmetics, and Dietary Supplements contract manufacturer. In addition, Tapemark is DEA registered as a Schedule II– V Manufacturer of Controlled Substances. Supporting its expanding global reach, Tapemark's quality system has been successfully audited by the European Union, Japan, Australia, and Korea, with CE mark certification.
Sub-EventZoneStand No
40C37
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
Sub-EventZoneStand No
40D33