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151-165 of 166 results
A New Approach to Outsourced Drug Development
| By INC Research
A perfect storm is forming within the biopharmaceutical industry. With a growing number of blockbuster drugs losing patent protection, clinical research executives are under immense pressure to bring new drugs to market. As sponsor companies struggle to replace the revenue loss threatened by generics, drug development is becoming more complex and expensive.
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Reducing Risk with the Right CRO Partner
| By INC Research
For drug developers, finding the right patients, investigators and outsourcing partners is essential. With shareholders demanding improved efficiencies, the resources, reach and expertise of a contract research organization (CRO) can expedite the research and development process.
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A New 384 Well Storage Plate Reducing Compound Consumption and Supporting Assay Miniaturisation
| By Greiner Bio-One
Technical notes and applications for laboratory work. Please download this free white paper for more information.
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Animal Models of Relapsing-Remitting Multiple Sclerosis
| By NEUROFIT
Relapsing-Remitting Experimental Autoimmune Encephalomyelitis (RR-EAE) is an animal model that mimics the initial courses of multiple sclerosis in humans. A rat model of RR-EAE is available at Neurofit. This model responds positively to anti-inflammatory / immunosuppressant drugs such as dexamethasone. For more information, please download this free white paper.
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Biovian - From Gene to Finished Vial
| By Biovian
Comprehensive information about Biovian, including detailed information on all services as well as examples.
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Biovian Company Brochure
| By Biovian
From gene to finished vial — Biovian is your one-stop-shop providing full range services in cGMP contract manufacturing of biologicals.
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Chinese Regulatory Changes for Human Serum and Plasma Exports Trigger Potential Delays
| By World Courier
Researchers conducting or planning to conduct clinical trials in China should be aware of new regulatory changes that specifically affect export shipments of human serum and plasma from China and the delays that the new administrative process may create. This free white paper includes a list of these major changes associated with the new regulations.
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Functional Imaging Using Computer Methods to Improve Respiratory Drug Development
| By FluidDA
Within the pharmaceutical industry it has become more and more apparent that the cost for the development of new products increases while the number of products that reaches the market declines. One of the causes for this phenomenon is the limited sensitivity of existing lung function tests to detect changes in pulmonary function in an early stage. Therefore within the field of respiratory medicine a consensus is starting to form around the need for new outcome parameters.
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Investigator Responsibilities Revisited by FDA
| By Norwich Clinical Research Associates
While the title of the new guidance from FDA is 'Investigator Responsibilities', in reality sponsors also have obligations since securing investigator compliance with applicable regulations is one of their legal obligations. To find out more, please download this free white paper.
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Latin America Emerges as World Competitor for Global Trials Despite Tough Regulatory Environment
| By World Courier
This article examines the regulatory atmosphere that prevails throughout Latin America and considers options that can streamline the timely flow of clinical trial materials through the supply chain.
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Live Cell Imaging of Drug Effects on Golgi Morpholgy Using the CELLview™ Cell Culture Dish
| By Greiner Bio-One
Fluorescent and time lapse microscopy, advantages of multiplex analysis and the Golgi apparatus. Please donwload this free white paper for more information.
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Spectral Unmixing for Hyperspectral Images of Breast Cancer Preparations
| By Carinthian Tech Research (CTR)
Scientific cancer research is based on the microscopic monitoring of cells and tissue. Now, methods of spectral image processing improve the image contrast and support medical diagnostics via software solutions.
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Taming China's Clinical Trial 'Dragon'
| By World Courier
With a population in excess of 1.3 billion and low technical costs, China is a highly attractive venue for clinical trials. In this article, current regulations and permit requirements are examined and a transportation case study is presented. Local solutions and important considerations for choosing appropriate "in country" service providers are also discussed.
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The Urgent Need for Qualified Transportation Providers in Global Clinical Research
| By World Courier
In light of sobering statistics from the MHRA, WHO and others about the quality of temperature-controlled drugs and medicinal products arriving at global research sites, regulatory agencies and pharmaceutical companies alike are demanding that every party involved in the pharmaceutical supply chain conform to GxP guidelines. This article outlines the main precepts of GxP as it applies to the pharmaceutical transport industry and offers insight on securing the global CTM supply chain.
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Animal Models of Cognitive Dysfunction
| By NEUROFIT
Three instrumental in-vivo assays for assessing the efficiency of drugs for the treatment of cognitive deficits are available at Neurofit. These assays can also be used to assess the side effect of drugs on memory (safety pharmacology).
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