Open access literature databases for mandatory drug safety literature screening during clinical development and post market 芒聙聯 equal access to new science for pharmaceutical companies.
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Copyright: © 2020 . This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Statement of the Problem:
It is difficult and expensive to meet the regulatory requirements in Europe and USA using existing commercial providers. Regulatory agencies mandate frequent often weekly literature searches using widely used reference databases. In addition, the European Union require literature searches in local language in member states. For many small or midsize pharmaceutical companies, the current costs for access to commercial reference databases and articles is prohibitive.
Methodology & Theoretical Orientation:
To conduct the required literature searches normally a subscription is required to access to commercial databases where the cost can run tens of thousands annually. Access to the full text articles must be paid separately which typically cost between $20-100 to access pr. article. Most existing library databases are not designed to support the specialized type of search that is required for drug safety to produce expedited single case reports and aggregate reports where searches are in date sequence and articles should be presented in a tabular format to quickly review the relevance of the article and access the full text as needed.
