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Clinical Trials White Papers

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121-135 of 138 results
CYNCRON - an Overview
| By CYNCRON
CYNCRON is a Nordic full-service clinical contract research organisation (CRO) with more than 25 years of experience, operating throughout Denmark, Sweden, Finland and Norway. We offer solid know-how and experience of clinical research, data management, biostatistics, pharmacovigilance and DMC/DSMB services for global and small pharma, biotech and medical device companies.
Contract Research & Services > Clinical Trials > White Papers
CYNCRON - a Full-Service Nordic Clinical Research Organisation (CRO)
| By CYNCRON
A data monitoring committee (DMC) / data safety monitoring board (DSMB) is an independent group of experts that monitors data from an ongoing clinical trial and gives recommendation to the sponsor regarding the best action to take. Cyncron can offer a range of DMC solutions ranging from assisting you in setting up the DMC with a charter, arranging meeting, delivery of packages to agreed timelines, and contact between the sponsor and the DMC.
Contract Research & Services > Clinical Trials > White Papers
Certainty Within Clinical Development
| By CYNCRON
There’s nothing like being sure. Especially in complicated projects where everything depends on the quality of the research. At Cyncron, our focus is to ensure that you have the conclusive information you need to make the right decisions. We are happy to provide credentials from other customers.
Contract Research & Services > Clinical Trials > White Papers
Biotechnology Solution Brief
| By Brainloop
Biotech companies need to share highly confidential documents in parallel with multiple prospective licensing partners — some who may be competitors — while ensuring that none of these proprietary documents are compromised during the process.
Contract Research & Services > Clinical Trials > White Papers
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.
Contract Research & Services > Clinical Trials > White Papers
Document Compliance Management
| By Brainloop
A DCM system covers the entire lifecycle of a document with no gaps. As a consequence, the document always remains under the system's watchful eye, even when it is opened, edited or stored on the desktop.
Contract Research & Services > Clinical Trials > White Papers
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.
Contract Research & Services > Clinical Trials > White Papers
Global Compliance for Medical Device Industry: Who needs Compliance to CFR, ISO13485, JPAL, D-MAH or 9100?
| By ENNOV
Medical device companies of all sizes face real challenges from emerging markets and international compliance. Many of the worlds regions are going through transformations where countries are making decisions to control their own destiny with respect to the standards and the requirements for regulatory compliance. Going, going, going gone are the days when other countries will accept the US standards and policies for managing the compliance or RAQA requirements.
Contract Research & Services > Clinical Trials > White Papers
Identifying and Exploiting Opportunities for Pharmacogenetics and Other Predictive Factors
| By Exploristics
Exploristics offer practical analysis tools that are built on basic principles and allow the evaluation of opportunities for PGx. This evaluation can be performed before the initiation of an extensive and costly experiment.
Contract Research & Services > Clinical Trials > White Papers
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.
Contract Research & Services > Clinical Trials > White Papers
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.
Contract Research & Services > Clinical Trials > White Papers
Management and Analysis of Biomarker Data
| By Exploristics
There is great expectation in the Pharmaceutical Industry that the era of personalised medicine will deliver safer and more effective treatments (Jørgensen & Winther, 2009). This promise is made possible by the emergence of new technologies and data acquisition platforms that can generate enormous amounts of patient-level biomarker data to characterise biological processes and explain response to treatment.
Contract Research & Services > Clinical Trials > White Papers
Peptide Professionals
| By PolyPeptide Group
This free comprehensive brochure gives details on The PolyPeptide Group including information on services provided.
Contract Research & Services > Clinical Trials > White Papers
Protecting Sensitive Information in Life Sciences Organisations
| By Brainloop
Critical business processes in biotech companies involve highly confidential, important documents that need to be safely accessed by external partners and potential licensees. Find a new way to protect this confidential documents.
Contract Research & Services > Clinical Trials > White Papers
Seamless Life Sciences Collaboration
| By Brainloop
Speeding up your time to market: Seamless online collaboration in the biopharmaceutical industry
Contract Research & Services > Clinical Trials > White Papers
121-135 of 138 results