| Clinical Consulting Services Pharmaceuticals_and_biotechnology > Consulting services > Clinical Consulting Services |  |
A global, full service CRO for drug, biological and device challenges.
Development in an effort to align the goals of scientific clinical research and fiscally responsible healthcare provision.
Drug discovery company focused on finding new therapeutic agents to treat diseases where there is an unmet clinical need.
Whether informing clinical trial program development, supporting marketing programs, or providing key clinical inputs to pharmacoeconomic analysis, MetaWorks delivers fast, objective, quantifiable answers founded on the most rigorous methodologi.
Consulting company for the pharmaceutical industry and a contract service laboratory.
Pan-European contract development organisation providing pre-clinical and clinical product development and safety services for the pharmaceutical and chemical industries
Development services for emerging technologies in the drug, biopharmaceutical and medical device industry.
Medeval is dedicated to the early clinical development of medicines
Based in Maryland, international full-service clinical research organization (CRO), accelerating the development and regulatory approval of new products.
Comprehensive consulting and contract research activities for the health sciences industry.
Serving the Salt Lake City community for over a decade providing research in health care.
Clinical trials management, regulatory and submissions consultancy.
Consulting specialization consisting of pharmaceutical chemistry, contract research and development, consulting, and flavor analysis.
Medical and scientific writing for the pharmaceutical, biotechnology and medical device industries.
Services include assay development and assay optimization, ultra High Throughput Screening (uHTS), as well access to discovery libraries.
Expert technical consultation in the areas of FDA Related Activities, Quality Control, Quality Assurance, Validation, Qualification, Stability and Expiration Dating.
Consulting services in clinical trials, regulatory affairs, and medical writing.
An organization offering medical and scientific writing for all phases of pharmaceutical and biotechnical clinical development.
A consortium of independent consulting specialists that offers experience and expertise in a number of functional areas for the development and operation of biotechnology, pharmaceutical and medical device companies.
Manufacturer of biotechnology instrumentation and the AccuTag(tm) combinatorial chemistry system. Products are sold to the pharmaceutical, biotechnology and education industries. This company was capitalized by venture capital.
Provides comprehensive program development for the pharmaceutical, biopharmaceutical and medical device industries.
Medical device egineering and market research consulting company, specialize in early stage engineering design, prototyping, and testing and market research for new device concepts.
Provider of organic and inorganic chemical testing services of consumer products. The company also provides method development and validation services. Services are provided to multiple industries.
Jan provides freelance clinical research services to the pharmaceutical industry and contract research organisations.
The innovative LAS expert system assists clinicians and clinical laboratories with the ordering and interpretation of laboratory tests to enhance diagnosis and control utilization.
Parent/holding company with high-tech units involved in pharmaceutical testing and consumer products testing services. This company was capitalized by private investment and venture capital.
BioPharmaceutical and Analytical equipment supplier, consultation in investment recovery, and R&D services.
We provide topical pharmaceutics (including pharmaceutical consulting), analytical services, topical manufacturing, and clinical labeling and packaging.
Matierials Characterization Analytical Laboratory for Analysis of Polymers, Plastics and Pharmaceuticals
Providing assistance to domestic and international Pharmaceutical Industries in the area of clinical research and regulatory affairs.
Services in data management, SAS programming, biostatistics, clinical site monitoring and clinical project management.
One of our key services is providing training for clinical research professionals, both on-site and in regional training classes.
PIA provides integrated product development services including regulatory consulting, clinical development, and medical writing support to the global health care industry.
Services in clincal testing and new product development.
Services range from analytical and microbiological services to support product development and marketed-product testing needs, to assistance with product submissions and post-approval support
Research and development organization specializing in protein electrophoresis and phoretix gel analysis software. Services include separation of proteins by 2-D and slab gel electrophoresis. Products and services are provided to academic and i.
Consulting, analytical, and custom research services related to the analysis and characterization of pharmaceutical solids.
Full service contract regulatory compliance consulting agencies to the Biotechnology, Pharmaceutical, Medical Device, Food and Cosmetic industries.
Research and consulting company providing services to the pharmaceutical industry and healthcare organizations.
Specialists in pharmaceutical and healthcare registration strategy, product development, preclinical and clinical research, regulatory support and training.
Designs and directs specialized clinical trial education programs that streamline and accelerate patient recruitment into specific clinical trials.
Research-based clinical reference laboratory which develops and provides incisive diagnostic, prognostic, and monitoring services to thousands of clients nationwide and in 10 foreign countries on 5 continents.
Clinical trial patient recruitment. We provide complete, creative marketing communications solutions for the healthcare medical marketplace.
An international certification organization, TUV is a EU Notified Body providing CE marking assistance, testing and certification for EMC, machinery and electrical, medical devices.
Company providing drug discovery services with proprietary drug discovery technologies.
Engaged in development and production of combinatorial compound libraries, lead finding processes in order to develop novel therapeutics against cancer, infectious deseases and other widely distributed illnesses.
Laboratory and clinical services, biochemical genetics testing, cytogenetics studies (chromosome analysis) and DNA diagnostic testing.
Contract organization for medical, biotechnology, and in vitro diagnostic device companies in CE Marking, design and development, clinical trials, QA, regulatory, reimbursement.
Pharmacokinetics, pharmacy, and metabolism software, along with research and cosulting services.
Sydney based organisation specialising in the provision of evidence-based consultant services to the health care sector.
Development of decision support technologies designed to speed the clinical research enterprise.
MAJARO has brought together a highly trained cadre of personnel who exemplify our commitment to providing our clients with unsurpassed clinical trial and technical expertise.
Australia-based CRO, specializing in providing services to the pharmaceutical industry.
European pharmaceutical agency whose areas of expertise includes antivirals, cardiology, hematology, gynecology and obstetrics, immunology and metabolic disorders.
Listing of Contract Research Organizations (CROs) and the Support of Clinical Trials.
Core competencies include business development, R&D management, information technolgy and regulatory affairs
Provider of coagulation reference services and medical consulting services. Services are provided to the medical industry. This company was capitalized by private investment.
Full-service contract research organization for pharmaceutical and biotechnology device industry
Provider of microbiology, analytical chemistry, toxicology testing, pharmaceutical nanosphere formulation, biocompatibility testing, contract sterilization and biotechnology research and development services; and manufacturer of biological indic.
A consulting group specializing in the pharmaceutical, biotechnology, and medical device industries for international business and clinical development.
UK-based engineering and project management company mainly involved in serving the pharmaceutical industry; services include: feasibility studies, process control automation, validation, clean room design, safety studies, process design and othe.
Team of topnotch scientists, quality assurance specialists, engineers, and technicians replete with the skills that can help bring products to market.
Resource Solutions, Inc. (RSI) provides comprehensive trials management, monitoring, medical monitoring, and QA auditing services in support of complex clinical drug and device research.
Contract research services including project management, data management, and QA consultancy.
Provider of lead-optimization services, screening libraries and licensing agreements.
Regulatory Strategies, Expert Reports, Clinical/Preclinical Overviews, CTX/IND, Plant Master Files, and Drug Master Files are just some of the services provided.
Information on research tools, genomic services and regulatory consultancy.
Specializes in consulting, contract research in the areas of the lab scale fermentation technology and downstream processing. Also offers technology transfer for the production of active pharmaceutical ingredients.
Serving the pharmaceutical and biotechnology industries with expertise in bioanalytical chemistry, pharmacokinetics, toxicokinetics, drug metabolism, drug delivery, and toxicology.
Provides wireless and handheld solutions for the pharmacuetical and biotechnology industries. In addition, provides web design, development and application hosting services.
Provides pharmaceutical, biotechnology and medical device companies assistance in monitoring Phase I-IV clinical trials.
Assisting clients in bringing new pharmaceutical products to market, by developing efficient scientific regulatory strategies that reduce the overall development time for new pharmaceutical products
Independent Review Board meets weekly for the thorough ethical review of clinical research studies. The IRB staff strives to process resulting documents within 72 hours of each meeting.
Provides R&D and technical services on a contract basis to clients primarily in the agrochemical, specialty chemical, and pharmaceutical industries.
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