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Benefit from industry communication professionals

Thomson Scientific can provide a comprehensive range of pharmaceutical communication support, from publication planning to medical writing, all tailored to the needs of the global pharmaceutical community. Our services span drugs, devices and biologics.

Improve the planning and execution of your communications

Our industry experts can help you fashion your clinical and non-clinical data — no matter what the scope and quantity — into concise, industry-standard formats that communicate the essential information to your target audience quickly, accurately, and in the language they expect.

Since 1990, we have focused on supporting the pharmaceutical development process. As part of The Thomson Corporation, we are able to draw on the best available scientific information, and apply unique evidence-based analysis. All our writers are skilled scientists, able to handle all aspects of preparing and executing successful and relevant communication programs.

We can save your company time, and work within your budgets, by identifying time and cost-saving opportunities early in the product development process. Our commitment to meeting your internal goals, and our attention to personal service, can provide a cost-effective alternative for your industry outsourcing needs.

Regulatory writing and consulting

We can help you to navigate the regulatory hurdles associated with product development and to facilitate approval of submissions by international regulatory authorities. We have participated in the design and preparation of more than 125 submissions, spanning even the most complex therapeutic areas.

Find out more information

Contact us today.


Further information

Click here to download the Thomson Pharmaceutical Services fact sheet

 

Areas of expertise
  • Regulatory writing support
  • Regulatory strategy and consulting
  • Quality assurance auditing
  • Publication planning
  • Integrated communication programs
  • Product awareness and understanding

We can help you to
  • Write INDs and CTDs
  • Design and validate regulatory strategies
  • Assure consistency and quality of submissions
  • Design integrated publication plans
  • Prepare manuscripts for publication
  • Create posters and presentations

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