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Identify and report significant effects

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Expert, confidential data retrieval, analysis and formatting

It is important to be alert to relevant information associated with your products. Regulatory authorities such as the FDA, CIOMS, and MHLW require you to search scientific and medical publications and report any identified adverse effects.

No other research service can match the global reach, attention to detail and high level of customization offered by Custom Information ServicesSM. No other pharmaceutical industry solution brings together so much expertise in data searching, indexing, abstracting, translating, analysis and formatting.

The Custom Information Services team includes more than 40 information specialists with advanced degrees and relevant experience. Before starting a project, they will work with you to analyze your goals and information needs and create an exclusive data profile for your organization. The team will determine the depth and breadth of your coverage and the specific criteria for relevancy to be applied to each article.

They will prepare a comprehensive specifications guideline document that details the scope of the project, including prioritization schedules for the completion and delivery of the various types of articles.

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Further information

Click here to download the Custom Information Services fact sheet

 

Can help you to
  • Demonstrate due diligence
  • Comply fully with pharmacovigilance responsibilities
  • Populate your proprietary literature databases including safety
  • Respond promptly to product-related inquiries
  • Collect and analyze competitive intelligence
  • Provide a front-end interface and data repository
  • Stay current in your field

Who can benefit
  • Regulatory affairs professionals
  • Medical professionals
  • Contract research organizations
  • Pharmaceutical companies
  • Biotechnology companies
  • Medical device companies
  • Regulatory authorities
  • Law firms

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