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Cro research - Import export

15 Companies

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ETHICAL GMBH

Switzerland

Ethical Grew Up With the eClinical World and Introduced eAdjudication® Solutions to It. Beginning as eClinical developers, our staff gained experience spanning the range of the eClinical world: eClinical technology, clinical systems, and data management in global trials, clinical trial quality and data compliance, and of course, endpoint adjudication (CEC). We gained the experience in successful engagements with academic research organizations (AROs), biopharmaceutical or medical device enterprises, clinical research organizations (CROs), and independent review committees. We have become expert in the creation, performance, and management of the Endpoint Adjudication process workflows and forms validation, private health information management and compliance, clinical trial and GxP compliance, clinical systems design, integration, and management, as well as web and mobile interface design. eAdjudication® is a Managed Software Service built over a single-purpose enterprise technology platform that supports every operation related to endpoint adjudication committee (CEC) management, contributing to the process best practices, quality control, and the flexibility to adapt to any scenario. eAdjudication® software integrates easily and is compatible with any EDC system. Ethical optimizes it for any study needs in any phase, for any SOPs, or to meet specific regulatory needs.

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PHATOPHY

France

Phatophy is a Contract Research Organisation established in Lyon since 1981. Phatophy offers to sponsors and clients from human and veterinary pharmaceutical/biological companies, biotechs and academic laboratories comprehensive services from proof of concept to regulatory studies throughout the whole development of your candidates, projects, products, medical devices and feed additives. Phatophy has developed expertise and excellence in different activities: Pharmaceutical development (analytical development, quality control, stability studies); InLife studies (preclinical studies); BioAnalysis; Regulatory Affairs and Project ManagementPhatophy is GLP accredited by ANSES French National Agency. Phatophy has Research Tax Credit agreement for the coming years. This agreement, obtained from the French authorities, permits to the clients working with Phatophy to refund R&D expenses to their corporate taxes. Phatophy is a member of www.lyonbiopole.com network. Phatophy est une CRO (Contract Research Organization) indépendante de prestations de services pour l’industrie pharmaceutique humaine et vétérinaire, les fabricants de dispositifs médicaux, les Biotech / Medtech, les fabricants d'aliments médicamenteux, les fabricants de cosmétiques... Développement et validation de méthodes d'analyses, études de stabilité, contrôle de qualité, études précliniques et cliniques, expertise réglementaire, conseils en management de projets R&D.
SYNTAX FOR SCIENCE S.L.

Spain

Syntax for Science is a Contract Research Organization (CRO) specialized in biostatistics and data management services for clinical studies providing support in all phases of clinical development.With presence in Spain and Switzerland, and 10 years of experience supporting clinical studies, we offer the experience of an international company with the tailored service of a local enterprise. As a technology based company actively involved in the scientific community, Syntax for Science use state-of-the-art methods and systems in biostatistics and data management. Our programming platform is developed in SAS v9.3 and follows international regulatory guidelines, so that your project is assured of validity and reproducibility (GAMP 5).
ICRC WEYER GMBH

Germany

ICRC Weyer is a Berlin based contract research organizatiom (CRO). The portfolio of the company contains high quality biostatistics, clinical data management and medical writing among other specialist services in the fields of medical research. The company conducts all provided services inlcuding all types of clinical trial projects from their Berlin offices. The highly qualified staff delivers valuable results for all trial phases, regardless of whether they are executed locally or globally. Furthermore, sponsors and partner CROs benefit from many years of experience as well as the delivery within period and budget. ICRC Weyer is a member of MEDIS RESEARCH GROUP. The group works closely together with selected partners to manage entire trial projects by providing full services, including site selection, recruitment, study conduct and monitoring within Europe, the U.S., Russia and parts of Asia.
SOFPROMED

Spain

Sofpromed is a technology-based full service contract research organization (CRO) specialized in the integral management of phase I-IV clinical trials, observational studies and research projects. The service portfolio of Sofpromed includes regulatory affairs, study start-up, site activation, enrollment support, monitoring, data management, logistics management, pharmacovigilance, biostatistics, medical writing and project management. The company develops customized electronic Case Report Forms (e-CRF).

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QUANTUM CHIMICA LTD.

Slovenia

Quantum Chimica is an European Contract Research Organization (CRO) offering regulatory affairs services worldwide. We have many years of experience in preparing CMC packages for CEP, DMF, ANDA and other applications within global regulatory environment. Our experience derives from very experienced and dedicated team of regulatory affairs managers, scientists and managers with in-depth knowledge of Organic and Analytical Chemistry, Biochemistry and Genetics, Pharmacy, HR and Sales management. Our team of experts holds university and post-graduate degrees and is efficient, professional and goal-oriented. We speak many foreign languages. Quantum Chimica is a trust-worthy partner that can help you set regulatory strategies and research activities as well as organize sales and marketing operations on local (EU) and international markets. We guarantee quality, efficient, fast and professional services following current good practices (GxP) and latest regulatory requirements.
ACCELERO BIOANALYTICS

Germany

Accelero Bioanalytics is a contract research institute (CRO) for the biotech industry experienced in the bioanalytics of nucleic acid therapeutics. Accelero Bioanalytics services comprises, but are not limited to: sandwich ligand binding assays, Real-Time RT-qPCR, hybridisation assays, and immunology assays for the pharmacokinetic and pharmacodynamic research on microRNA, miRNA, siRNA, aptamers, antisense oligos, CpG oligos, transcripts, etc. in prelinical/clinical drug development. Accelero Bioanalytics services are fully compliant to Good Laboratory Practice (GLP). Our customers benefit from more than 10 years experience in the bioanalytics of microRNA, miRNA, aptamers, and antisense oligos. Accelero Bioanalytics is proud to be one of the first in Europe to offer GLP compliant Real-Time RT-qPCR for microRNA bioanalytics.
ANNICK DEFLANDRE TRIAL SERVICES (ADTS)

Belgium

Annick Deflandre Trial Services is a small independent CRO (Clinical Research Organization) / SMO (Site Management Organization) created in 2000 by Annick Deflandre. ADTS is dedicated to provide you with clinical research services compliant with the latest ICH-GCP guidelines. We offer flexible efficient reliable and experienced clinical research services.
IPM BIOTECH GMBH

Germany

IPM Biotech is a cutting-edge, science driven specialized bioanalytical contract research organization (CRO). We develop assays to support drug developing companies in their drug development programs. IPM Biotech works strictly in compliance with GLP regulations.
VERUM.DE GMBH

Germany

Verum's core business and key competence is Full Clinical Service for Phase II to IV in CEE countries. Verum has been the first Western-Standard CRO specializing in CEE countries.

DMMBLITZ

United Kingdom

We are an international digital marketing agency near York in the United Kingdom, offering the following online marketing solutions: -Website Design & Development -SEM / PPC -Search Engine Marketing -CRO - Conversion Rate Optimisation -SMM - Social Media Marketing -SMO - Social Media Optimisation -SEO - Search Engine Optimisation -YouTube & Display Network Marketing -eMail & SMS Marketing -Branding & Design -Content Marketing -Managed Cloud Hosting -Business Signage -Bespoke & Custom Maps Let us take care of your digital marketing, while you do what's most important, focus on your business. Starting out as a market research and website design agency in 2013 we now cover all aspects of digital marketing. From website development to google ads, pay per click including google adwords PPC and social media marketing, we'll give your online marketing the complete blitz. The planning and implementation of digital marketing agency services can be broken down into the three steps defined below. At DMMBlitz we can become engaged with your business at any point in the online marketing journey. Be it strategy consultation, research and development, creative design, implementation, monitoring and management. 1. Consultation 2. Development & Implementation 3. Management & Monitoring Contact us now for an unbeatable price!

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SPACE & TIME MEDIA LTD

United Kingdom

Space and Time is an award winning independent media planning and buying agency with offices in London, Surrey, Manchester and Edinburgh and a raft of experience in all media channels and disciplines. Experts across all media channels, we specialise in the provision of well-researched, fully integrated and beautifully crafted media campaigns. With clients across healthcare, retail, property, finance, leisure and tourism, you may have seen some of our work. The scope of our work takes in online and offline media, including paid search (PPC), SEO, CRO & advanced analytics, display, video, content management and special builds, as well as print, out of home, broadcast, leafleting and data provision. As well as being experts in our own field, we like to get under the skin of yours. Only by properly understanding your industry and your position within it can we deliver the kinds of insight needed to plan media properly. We begin planning only when we know what success looks like and how it will be measured. Get in touch if you’d like to discuss how we can help you.

BIO BENCH

Belgium

Bio Bench co. ltd (www.bio-bench.com) - A one-stop-shop CRO active in the generation of functional antibody and bio-active protein for drug discovery, IVD kit and biological research. Founded by a group of innovative-spirit-driven biologists in 2013, Bio Bench team has solid know-how and a passion for improving our integrated CRO platform. Bio Bench developed numerous in-house SOPs to provide researchers the most cost-effective and high quality services from sequence to pilot scale production. Bio Bench’s vision: bring functional and bio-active antibody/protein into early stage discovery to minimize the risk for your project. High-lighted one-stop-shop project: -Drug discovery - from sequence to drug antibody. -IVD kit development - An application guaranteed service. Featured service: -Human naïve antibody library 100-billion clones - directly find your drug potential antibody with human sequence. -Antibody Cell line and production - from 1mg/L to 4000mg/L, from 0.1L to 200L. -Guaranteed antibody service - WB, flow cytometry, Sandwich ELISA and IF. -Bi-specific antibody - The function and the beyond.
GEORGE CLINICAL CRO

United Kingdom

We are a leading CRO in the Asia-Pacific, with global capabilities, providing quality clinical trial research services from start to finish; augmented by science and innovation. George Clinical is a leading research organisation in Asia with over 300 global staff. George Clinical provides the full range of clinical trial services to pharmaceutical, medical device and biotech customers, for all trial phases, registration and post-marketing trials. George Clinical combines scientific and clinical leadership with expert trial delivery capability to create a distinctive world-class service. George Clinical is a leading clinical contract research organisation company in Asia with over 300 global staff. George Clinical provides the full range of clinical trial services to pharmaceutical, medical device and biotech customers, for all trial phases, registration and post-marketing trials. George Clinical combines scientific and clinical leadership with expert trial delivery capability to create a distinctive world-class service CRO.
EUROMEDEX

France

EUROMEDEX works in accordance with pharmaceutical standards and proposes the following services: * International Pharmaceutical Wholesaler: more than 200.000 drugs, medical devices, cosmetics and food supplements available for sale on the international market. Daily, on request, EUROMEDEX provides them worldwide. * Pharmaceutical Export Development: with our own representative offices located in Eastern Europe, Central Asia and Caucasus Countries. Closely with Marketing Authorization Holders, 120 skilled EUROMEDEX people are carrrying out initial market research, regulatory affairs, promotion, pharmacovigilance, export from France and distribution on the field. * Pharmacovigilance: EUROMEDEX Safety Department proposes to partners a customized and outsourced solution, from collection of individual case safety reports to transmission to competent authorities. * Clinical Trials Logistic: EUROMEDEX Clinical Trial Logistic proposes a tailored service to CROs and clinical promotors. EUROMEDEX takes charge of all clinical trials logistic steps. * Life Science Products: EUROMEDEX Life Science Products is a distributor of high quality reagents for research use. Working closely with a number of innovative manufacturers, EUROMEDEX offers a wide range of products in Molecular and Cell Biology, Immunology and Genetics.

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15 Companies